Ignite Creation Date:
2025-12-25 @ 2:00 AM
Ignite Modification Date:
2026-02-28 @ 11:18 AM
Study NCT ID:
NCT02129894
Status:
UNKNOWN
Last Update Posted:
2014-05-02
First Post:
2014-04-30
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
The Use of Abdominal Binders in Patients Undergoing Cesarean Sections
Sponsor:
St. Luke's Hospital, Pennsylvania
Organization:
Study Overview
Official Title:
The Use of Abdominal Binders in Patients Undergoing Cesarean Sections: A Randomized Controlled Trial
Status:
UNKNOWN
Status Verified Date:
2014-04
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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.
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 Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: