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Search / Trial NCT00918996

The Bladder Flap at Cesarean Section: A Randomized Controlled Trial

Launched by WASHINGTON UNIVERSITY SCHOOL OF MEDICINE · Jun 9, 2009

Trial Information

Current as of November 05, 2025

Completed

Keywords

Cesarean Section Bladder Flap Operating Time

ClinConnect Summary

BACKGROUND

Cesarean section is the most common major surgical procedure in women world wide. In the United States almost 25% of deliveries are by cesarean section and the rate continues to rise \[1\]. In performing this procedure, it is imperative that evidence based techniques are utilized to optimize outcomes and minimize complications. Recently, the case has been made for simplifying the procedure by eliminating unnecessary and potentially harmful steps \[2\].

Rationale for the Bladder Flap Challenged: While the creation of the bladder flap has long been an integral part of the standar...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Patients undergoing non-emergent primary and repeat cesarean sections at or greater than 32 weeks gestation at Barnes Jewish Hospital during the study period.
  • Exclusion Criteria:
  • Emergent cesarean sections, planned vertical uterine incision, previous abdominal surgeries (besides prior cesarean sections), sedation and inability to obtain consent.

About Washington University School Of Medicine

Washington University School of Medicine is a leading academic medical institution renowned for its commitment to advancing healthcare through innovative research, education, and patient care. With a strong emphasis on translating scientific discoveries into practical applications, the institution conducts a diverse array of clinical trials aimed at improving treatment outcomes and enhancing the understanding of various medical conditions. Its collaborative environment fosters partnerships between researchers, clinicians, and community stakeholders, ensuring that the trials not only contribute to scientific knowledge but also address the pressing health needs of diverse populations.

Locations

St Louis, Missouri, United States

Patients applied

0 patients applied

Trial Officials

George A. Macones, MD, MSCE

Principal Investigator

Washington University School of Medicine

Methodius G. Tuuli, M.D., M.P.H.

Principal Investigator

Washington University School of Medicine

Anthony Odibo, MD, MSCE

Principal Investigator

Washington University School of Medicine

Patricia Fogertey, BSN, MSN

Principal Investigator

Washington University School of Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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