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NCT07846930Not yet recruiting

Timing of Cesarean Wound Dressing Removal on Wound Healing in Women With BMI ≥ 30 kg/m²

Effect of Cesarean Wound Dressing Removal Timing on Wound Healing in Women With BMI ≥ 30 kg/m²

Source: ClinicalTrials.gov · Last updated 29 Sept 2026

Brief summary (registry, in English)

Cesarean delivery is one of the most common surgical procedures in obstetric care. Women with obesity (body mass index \[BMI\] of 30 kg/m² or higher) are at increased risk for postoperative wound complications, including surgical site infections, fluid collections (seroma/hematoma), and wound separation. Postoperative wound dressings protect the surgical incision, but the optimal timing for dressing removal remains uncertain, particularly for high-risk patients. The purpose of this prospective cohort study is to compare wound healing and the occurrence of surgical site infections between two standard dressing removal schedules in women with a BMI ≥ 30 kg/m² undergoing cesarean delivery. Participants are observed in one of two groups according to standard hospital practice: * Group 1: The sterile wound dressing is removed at approximately 48 hours after surgery. * Group 2: The sterile wound dressing is removed at approximately 5 days after surgery. Following dressing removal, incisions are assessed for signs of infection, drainage, swelling, and healing progress. The study aims to provide evidence on whether earlier dressing removal at 48 hours is safe and effective compared to delayed removal at 5 days in women with obesity.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
726 (estimated)
First submitted
23 Sept 2026
Start date
Oct 2026
Primary completion date
Oct 2027
Lead sponsor
Assiut University
Diseases
Obesity
NCT number
NCT07846930

What you commit to

  • Study type: Observational
  • Planned participants: 726
  • From Oct 2026 to the primary completion date, Oct 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Active systemic infection or fever prior to surgery
  • Major intraoperative contamination of the surgical field
  • Major postoperative complications requiring additional abdominal surgery

Other illness

  • Pre-existing infection or inflammation at the planned incision site
  • Significant preoperative bleeding or anemia
  • Known bleeding or coagulation disorders that may significantly affect wound healing

Other

  • Clinical or subclinical chorioamnionitis
  • Inability or unwillingness to attend scheduled follow-up visits

Who the study is looking for

  • Women aged 18 to 35 years
  • Body mass index (BMI) ≥ 30 kg/m² measured before cesarean delivery or at admission
  • Undergoing cesarean delivery with a Pfannenstiel skin incision and primary skin closure

Age in the registry: 18 years to 35 years · Sex: Female

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.