Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 2:00 AM
Ignite Modification Date:
2025-12-25 @ 2:00 AM
NCT ID:
NCT02129894
Brief Summary:
To see if the use of Abdominal Binders improves patients out comes after cesarean delivery
Detailed Description:
Inclusion: All patients admitted to labor and delivery
Consented patients who had a cesarean delivery will be randomized using a number table to receive or not receive an abdominal binder.
Outcomes: On postoperative days 1 and 2, patients were asked to complete a pain visual analog scale and the validated Symptom Distress Scale. Postoperative hemoglobin and hematocrit were also recorded.
Study:
NCT02129894
Study Brief:
Protocol Section:
NCT02129894