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Abdominal Binder Following Cesarean Delivery

Effect of Elastic Abdominal Binder on Pain and Functional Recovery After Cesarean Delivery: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03080506
Enrollment
180
Registered
2017-03-15
Start date
2017-04-18
Completion date
2017-12-12
Last updated
2018-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Section Complications

Brief summary

Cesarean delivery is a common obstetrical procedure and is associated with increased maternal morbidity and mortality. Pain and limited mobilization are major contributing factors that result in delayed functional recovery and complications. Elastic abdominal binder, a wide elastic belt that is wore around the patient's abdomen to support surgical incision after surgery, has been employed by clinicians for pain relief, wound complications prevention, improved pulmonary function, and stabilization. Benefits of the abdominal binder use have not been properly examined. The aim of this study is to examine the effect of postcesarean elastic abdominal binder use on recovery by comparing pain scores and mobility function (through the 6-minute walk test \[6MWT\]) in postcesarean mothers who use versus do not use the elastic abdominal binder to support incisional site.

Interventions

Participants will be fitted with an elastic abdominal binder at the time of procedure completion just before leaving the operating room. The binder will be placed snuggly tight on top of the hospital gown at the infraumbilical level with the incision positioned at the middle part of the binder. The patients will be encouraged to wear binders at all time. However, periods of break from wearing the binder will be allowed at their convenience.

Sponsors

Chiang Mai University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women undergoing cesarean delivery

Exclusion criteria

* Cesarean hysterectomy * Intraoperative accidental injury to urinary or gastrointestinal organs * Postoperative admission to intensive care unit (ICU) * Postoperative intraperitoneal drain placement * Unable to understand and follow oral/written instructions * Severe neuromuscular or circulatory disorders * Pulmonary diseases

Design outcomes

Primary

MeasureTime frameDescription
Daily average postoperative pain scoresAn average of pain scores at 8:00 am and 4:00 pm, up to 7 days postoperationA visual analog scale pain score
Postoperative functional recoveryIn the morning of postoperative day 3Six-minute walk test (6MWT)

Secondary

MeasureTime frameDescription
Quality of lifeIn the morning of postoperative day 3The EuroQol Group's ED-5D-5L questionnaire
Postoperative complicationsIn the morning, up to 7 days postoperationFebrile morbidity, wound complications, bowel ileus

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026