Recruiting
Phase 3

Abdominal Binders

Sponsor:

St. Luke's Hospital, Pennsylvania

Code:

NCT02129894

Conditions

Cesarean Section Post Operative Management

Eligibility Criteria

Sex: Female

Age: 18 - 50

Healthy Volunteers: Not accepted

Interventions

abdominal Binder

Study Details

Brief summary:

To see if the use of Abdominal Binders improves patients out comes after cesarean delivery

Conditions

Cesarean Section Post Operative Management

Study ID

NCT02129894

Start date

Nov, 2013

Status verified date

Apr, 2014

Completion date

Oct, 2014

Anticipated

Primary completion date

Sep, 2014

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 18 - 50

Healthy Volunteers: Not accepted

Inclusion Criteria:

Women undergoing cesarean section for any indication

Exclusion Criteria:

  • unable to give consent

Study Design

Enrollment

210 participants

Anticipated

Allocation

Randomized

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: abdominal binder

Post cesarean section patients will get a abdominal binder placed

no intervention: No Abdominal Binder

Post cesarean section patients will not have abdominal binder

Interventions

abdominal Binder

placement of abdominal binder

Primary outcome measure

  • Pain measurement [ Time Frame: up to post operateive day 2 ]
  • Patient Distress score [ Time Frame: up to post operateive day 2 ]

Central Contacts and Locations

Central contacts

James N Anasti, MD

484-526-4670anastij@slhn.org

Locations

St Luke's University Hospital

Recruiting

Bethlehem, Pennsylvania, United States, 18015

Contacts

James N Anasti, MD

484-526-4670anastij@slhn.org

Principal Investigator:

James N Anasti, MD

More Information

Sponsor

St. Luke's Hospital, Pennsylvania

Last update posted

May 2, 2014

Last verified

Apr, 2014

Keywords

  • cesarean section
  • postoperative pain
  • pregnancy
  • abdominal binder

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by St. Luke's Hospital, Pennsylvania on 2014-05-02.