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Urinary Symptoms and the Omission of the Bladder Flap at the Time of Primary Cesarean Delivery

N

National Naval Medical Center

Status

Completed

Conditions

Pelvic Floor Disorders

Treatments

Procedure: Bladder flap

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT02967913
2007.0005

Details and patient eligibility

About

The bladder flap at the time of cesarean delivery is the term used to describe the separation of the bladder from the lower uterine segment by sharply incising the vesico-uterine peritoneum or serosa and using blunt and/or sharp dissection to develop this potential space which facilitates placement of a retractor, known as the bladder blade. Creating a bladder flap at the time of cesarean delivery is largely based on individual practice patterns and practitioners are divided in their use of this step. While creating a bladder flap has a theoretical advantage of protecting the bladder from injury, it is unknown whether this step has an effect on postoperative bladder function. The purpose of this study was to evaluate whether the omission or creation of a bladder flap results in a change in urinary symptoms as measured by the UDI-6 component of the PFDI-20.

Full description

This is a Parallel Assignment design study. The PFDI-20 symptom questionnaire was completed upon enrollment. After the patient was prepped and draped, the operating room nurse opened a sealed opaque envelope marked with the study subject number containing a card marked with the assignment to bladder flap or no bladder flap, which was shown to the surgeons prior to the skin incision. The patient did not see the allocation nor was it verbalized in the operating room. The PFDI-20 was repeated 6-8 weeks after delivery at the patient's postpartum exam clinic visit. Equal number of bladder flap and no bladder flap assignment cards were randomly shuffled and placed in envelopes marked with the study subject ID number prior to the start of the study.

The study hypothesis was that the omission of the bladder flap at the time of primary cesarean delivery would be associated with lower urinary symptoms scores in the postpartum as measured by the UDI-6 component of the PFDI-20.

Enrollment

70 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • pregnant at 37 weeks gestation or greater
  • scheduled for a non-urgent primary cesarean delivery

Exclusion criteria

  • pre-term (defined as less than 37 weeks 0 days gestation) prior pelvic surgery involving the bladder
  • a diagnosis of any of the following conditions: endometriosis, uterine leiomyomata, chronic pelvic pain, urinary incontinence prior to pregnancy, nephrolithiasis during the current pregnancy,
  • any circumstance that precluded adequate informed consent at the time of recruitment (such as a need to for urgent or emergent delivery)
  • if the indication for cesarean was a failed trial of operative vaginal delivery (forceps or vacuum extraction)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

Bladder flap performed as per routine
Experimental group
Description:
Bladder flap surgical step performed at time of non-urgent primary cesarean delivery as per routine
Treatment:
Procedure: Bladder flap
Bladder flap is omitted
No Intervention group
Description:
No bladder flap performed at time of non-urgent primary cesarean delivery

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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