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This page tree describes how to abstract and edit the scientific details of clinical trials.

About Scientific Data

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Abstracting Trial Descriptions

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Abstracting Interventional Trial Design

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Abstracting Non-Interventional Trial Design

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Abstracting Outcomes

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Abstracting Eligibility Criteria

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Abstracting Diseases and Conditions 

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Abstracting Data Table 4 Anatomic Sites

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Abstracting Biomarkers

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Abstracting Interventions

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You can search for, and select, interventions from a stored list of active intervention terms extracted from NCIt and link them to a trial. NCIt is an online database developed and maintained by the National Cancer Institute Enterprise Vocabulary Services. You can find more detailed information about NCIt at http://ncit.nci.nih.gov/.

Additionally, Protocol Abstraction provides a structure for describing drug, radiation, and surgical procedure details. It generates a description from values you provide for such parameters as dose, target site, frequency of administration, etc.

Info
titleObsolete terms

Some intervention terms become obsolete over time. When you validate the trial, the system displays an error message if the abstraction contains an obsolete term. If this occurs, look up the intervention name and replace the obsolete term with the new one.

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titleCheck out the trial before you begin abstraction

Before you begin abstracting or validating any trial, be sure you check it out first. Otherwise you will not be able to modify any trial data.

Trials can have multiple intervention records. Each record displays the following information about the intervention:

Intervention data definitions

Column Name

Definition

Name

Standard name used to refer to each intervention. For drugs, this is the generic name. For investigational new drugs that do not yet have a generic name, this may be the chemical name, company code, or serial number.

Other Names

Synonym or other name

Footnote

Alternate names you record appear in the TSR and XML documents.

Description

For drug interventions, a summary of the drug’s chemical nature and (potential) mechanism of action, and/or details such as dosage form, dosage, frequency, and duration.
For other interventions, a summary of the procedure or device that provides key details that distinguish it from similar interventions.

Tip
titleTip

You can generate descriptions for drug, radiation, and surgical procedure interventions using Protocol Abstraction’s structured approach. To do so, see Generating Drug, Radiation, and Procedure/Surgery Descriptions.

Type

Mode of intervention, for example, drug or device.

Footnotes Display

Additionally, you can add, edit, reorder, and delete records.

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titleSorting intervention records

You can change the sort order (ascending/descending) of any column other than Edit and Delete by clicking the column name and selecting the up or down arrow that appears.

 

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 Adding Interventions

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You can link interventions to a trial by searching for an intervention name from the current list of active records.
The terminology list is refreshed weekly.

How to Add Interventions

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Click Add. The Add intervention page appears.
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In the Intervention Name field, type part or all of the intervention name.

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titleTip

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  1. To include synonyms in your search in addition to preferred names, select the Include Synonym check box.
  2. To limit your search to exact matches only, select the Exact Match Only check box.

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Optionally, in the Intervention Description field, enter the name/description of the intervention. 

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Although not displayed on the Interventions page, the system records the ClinicalTrials.gov code for the intervention.

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Generating Drug, Radiation, Procedure, and Surgery Descriptions

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Protocol Abstraction provides a structure for abstracting detailed descriptions of drug, radiation, and procedure/surgery interventions.

How to Generate Drug, Radiation, and Procedure/Surgery Descriptions

  1. Search for the trial of interest. In the search results, click the NCI Trial Identifier link for that trial.
  2. On the Scientific Data menu, click Interventions. The Interventions page appears, with or without any intervention records displayed.
  3. Click Add. The Add intervention page appears.
  4. From the Intervention Type field, select Drug, Radiation, or Procedure/Surgery as appropriate.

    Tip
    titleTip

    Do not type an intervention description at this point. The system automatically populates the Intervention Description from information you provide in the next steps.

  5. Follow the steps in Adding Interventions for instructions for searching for, and selecting, interventions.
    The Interventions page expands to display a Drug Information, Radiation, or Procedure Information section, depending on your selection.
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    Radiation Information section of Add Intervention pageImage Removed
    Procedure Information section of Add Intervention pageImage Removed
  6. In the Drug, Procedure, or Radiation Information section of the page, enter the values in the text fields provided.
  7. To provide values for the parameters that require harmonized terms (the gray fields), click Look Up.
    The Search window appears .
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  8. Type your search criteria in the field(s) provided, and then click Search. If the information you are abstracting includes a range, for example, dose range, you can provide the lower limit without providing the upper limit. However, do not provide the upper limit of a range unless you also include a lower limit.

    Info

    You must type at least one character in any of the search fields.

    The Search window displays the result(s) of your search.
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  9. In the search results list, locate the preferred item, and then click Select.
  10. Once you have provided information for all relevant fields, click Generate.
    The information you provided is displayed in the Intervention Description field.
    Add Intervention page annotated to show generated data in Intervention Description fieldImage Removed
  11. Click Save.

 

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Editing Interventions

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You can edit trial descriptions. However, if you need to change the intervention type or name, you must delete the record and create a new one with the correct information. See Deleting Interventions.

How to Edit Intervention Records

  1. Search for the trial of interest. In the search results, click the NCI Trial Identifier link for that trial.
  2. On the Scientific Data menu, click Interventions. The Interventions page appears.
    Interventions page annotated to show edit iconImage Removed
  3. In the Edit column for a given record, click the Edit (pencil) icon.
    The Edit Intervention page appears.
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  4. Edit or enter the intervention description, and then click Save.
    If you edit a drug, radiology, or procedure intervention, the Edit Intervention page displays the original form for the record.
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  5. To edit the intervention description and/or details of drugs, radiation, and procedures/surgeries, follow the instructions in Adding Interventions.
  6. Click Save.

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Reordering Interventions

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You can change the order in which the interventions are displayed in the interventions table and in the TSR/XML documents.

How to Re-Order Intervention Criteria

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Deleting Interventions

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When you delete interventions from a trial, you delete them from view, and can not recover them. If you delete a record accidentally, follow the instructions in Adding Interventions to add it back.

How to Delete Interventions

  1. Search for the trial of interest. In the search results, click the NCI Trial Identifier link for that trial.
  2. On the Scientific Data menu, click Interventions. The Intervention page appears.
  3. In the Delete column, select the check box for each record you want to delete, then click Delete. To delete all records, click Select All, and then click Delete.

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Managing Intervention Terms

You can import NCIt terms on demand if the term you require for abstraction does not exist in the CTRP database. Once imported, CTRP syncs the term with in the NCIt database automatically.

If a term does not exist (i.e., has not been published yet) in the NCIt, you can request the term directly from EVS. Once EVS curators have responded to your request, you can enter new term details when abstracting trials. Later EVS publishes the new term in the NCIt. Refer to Managing Disease and Intervention Terminologies.

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  1. At the bottom of the Interventions page, click Manage NCIt Terms.
    The Manage NCIt Terms menu contains options for managing intervention terms.
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  2. Follow the instructions in the following sections:

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Abstracting Arms 

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When adding arms to a trial, you assign to them the interventions currently abstracted for the trial.

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titleCheck out the trial before you begin abstraction

Before you begin abstracting or validating any trial, be sure you check it out first. Otherwise you will not be able to modify any trial data.

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  • There must be at least one arm/group that implies that the entire study subject population receives the same intervention.

  • The number of arms/groups added to the trial must coincide with the number indicated in the trial’s Design Details. See Abstracting Interventional Trial Design Details.

  • Every arm must have at least one assigned intervention (except for the arm type "no intervention").
  • Every intervention must be assigned to at least one arm.
  • There must be only one arm with the same combination of description and associated intervention.
  • Arm details for single-arm trials are not required.

Trials can have multiple arm records. Each record displays the following arm information:

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Field

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Definition

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Label

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Short name used to identify the arm or comparison group.

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Type

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Description

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Brief description of the arm or comparison group to distinguish it from other arms/groups in the trial.

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Assigned Interventions

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Intervention(s) assigned to a given arm.

Footnote

Interventions imported from ClinicalTrials.gov may not match CTRP terminology.


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Footnotes Display

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Adding Arms

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You can add one or more arms to a trial according to the trial’s design details.

How to Add Arms

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In the drop-down lists and text fields, select or enter the appropriate information. The following table describes the fields. An asterisk (*) indicates a required field.

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Trial Description

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Instruction

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Label*

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Type the descriptive name of the arm.

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Type*

Select the appropriate arm function. Valid values are as follows: 

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Arm Description

Type a brief description of the arm.

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Assignment

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For arm types other than No Intervention, select the check box in the column for the intervention assigned to the current arm.

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Editing Arms

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You can edit arm records as necessary.

How to Edit Arm Records

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Deleting Arms

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When you delete arms from a trial, you delete them from the system, and can not recover them.

How to Delete Arms

  1. Search for the trial of interest. In the search results, click the NCI Trial Identifier link for that trial.
  2. On the Scientific Data menu, click Arms. The Arms page appears.
  3. In the Delete column for the appropriate record, click the Delete icon.

    Warning

    There is no way to recover a deleted record. If you delete a record accidentally, follow the instructions in Adding Arms to add it back.

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Abstracting Groups and Cohorts

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Group/cohort information pertains to Complete non-interventional trials only. In non-interventional studies, cohorts are groups of individuals, initially defined and composed, with common characteristics (e.g., condition, birth year), who are examined or traced over a given time period.

When adding groups to a trial, you assign to them the interventions currently abstracted for the trial.

Info
titleCheck out the trial before you begin abstraction

Before you begin abstracting or validating any trial, be sure you check it out first. Otherwise you will not be able to modify any trial data.

The following rules apply to each trial:

  • There must be at least one group/cohort that implies that the entire study subject population receives the same intervention.

  • The number of groups/cohorts added to the trial must coincide with the number indicated in the trial’s Design Details. See Abstracting Non-Interventional Trial Design Details .

  • Every group/cohort must have at least one assigned intervention.
  • Every intervention must be assigned to at least one group/cohort.
  • A trial must have only one group with the same combination of description and associated intervention.

Trials can have multiple group/cohort records. Each record displays the following group information:

Field

Definition

Label

Short name used to identify the group

Description

Explanation of the nature of the study group (e.g., those with a condition and those without a condition; those with an exposure and those without an exposure).

Assigned Interventions

Intervention assigned to a given group

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Adding Groups

You can add one or more groups to a trial according to the number specified in the trial’s design details. See Abstracting Non-Interventional Trial Design Details .

How to Add Groups

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Field

Instruction/Description

Label*

Enter the descriptive name of the group.

Description*

Enter a brief description of the group.

Assignment

Select the check box(s) in the column for the intervention(s) assigned to the current group.

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Editing Groups

You can edit group records as necessary.

How to Edit Group Records

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Deleting Groups

When you delete groups from a trial, you delete them from the system, and can not recover them. If you delete a record accidentally, follow the instructions in Adding Groups to add it back.

How to Delete Groups

  1. Search for the trial of interest. In the search results, click the NCI Trial Identifier link for that trial.
  2. On the Scientific Data menu, click Groups/Cohorts. The Groups page appears.
  3. In the Delete column, select the check box for the appropriate record(s), and then click Delete.
  4. To delete all groups, click Select All, and then click Delete.

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Abstracting Sub-Groups

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Trials can have multiple sub-group records. Each record displays the following information about the disease or conditions:

Field

Definition

Code

Characters, or phrase used to identify the sub-group

Description

Stratification criteria

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titleCheck out the trial before you begin abstraction

Before you begin abstracting or validating any trial, be sure you check it out first. Otherwise you will not be able to modify any trial data.

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Adding Subgroups

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You can add one or more sub-groups to a trial according to the trial’s design details.

How to Add Sub-groups

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Editing Subgroups

You can edit sub-group records as necessary.

How to Edit Sub-group Records

  1. Search for the trial of interest. In the search results, click the NCI Trial Identifier link for that trial.
  2. On the Scientific Data menu, click Sub-groups. The Sub-groups page appears.
  3. In the Edit column for a given record, click the Edit icon. The Add/Edit Sub-group Information page appears.
  4. Modify the sub-group details according to instructions in Adding Sub-Groups.
  5. Click Save.

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Deleting Subgroups

When you delete groups from a trial, you delete them from the system, and can not recover them. If you delete a record accidentally, follow the instructions in Adding Sub-Groups to add it back.

How to Delete Sub-groups

  1. Search for the trial of interest. In the search results, click the NCI Trial Identifier link for that trial.
  2. On the Scientific Data menu, click Sub-groups. The Sub-group page appears.
  3. In the Delete column for the appropriate record, click the Delete icon.

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