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Delete item from question

The Study Designer application enables study teams to configure CRFs for clinical trial visits with a variety of tools. There are various form field options such as text fields, checkboxes, dropdown menus, date pickers, and more. You can place these fields on the form canvas, arrange them as needed, and make sure they are associated with the corresponding variables.

When maintaining a form, it may occur that some items need to be deleted from the question due to the updated protocol requirements or other reasons specified by the sponsor. Once the item is deleted, it will no longer be available on the form after it is published to EDC.

To delete an item from a form question

  1. In the Study Designer application header, select the CRF DESIGN tab.

  2. In the toolbar, select the latest draft CRF version marked with the respective unlock symbol unlocked_icon_purple.png, otherwise, you cannot perform any actions.

    Selecting latest draft CRF version
    Figure 1. Selecting latest draft CRF version

  3. In the left pane that appears, expand the unique form directory of any visit. Then select the needed form.

    Important

    Note that by updating a unique form, you introduce changes to all visit forms linked to it and vice versa.

    Accessing form to configure
    Figure 2. Accessing form to configure

  4. On the form content page that appears, next to the needed item, select More icon_more_actions.png > Delete trash_can_icon.png.

    Selecting option to delete item
    Figure 3. Selecting option to delete item

    Important

    When dealing with the checkbox item, the Delete option is intended for the removal of a single checkbox option. To delete the entire checkbox item from the question, you need to select Delete Checkbox Group trash_can_icon.png.

  5. In the Delete Item confirmation dialog that appears, select button_delete.png to confirm your action.

    Confirming item deletion
    Figure 4. Confirming item deletion

Once confirmed, the item is deleted from the question. You can now continue to maintain forms with available actions.

In this section:

A specialized document in a clinical trial designed to collect the subject data.

See also eCRF.

Any person, company, institution, group, or organization that is a client of EDETEK and a user of the eClinical system.

In the eClinical system, the Sponsor role is assigned to the user who oversees or pays for a clinical trial and collects and analyzes the data. Before the study goes live, the Sponsor users work closely with the data managers, configuring CRFs and other aspects to make sure everything meets their requirements before giving the green light for the study to go live. In the course of a trial, the Sponsor users make requests for amendments in the system according to a new protocol version, changes in business requirements, or other needs.