Bladder Flap Technique In Elective Cesarean Section

NCT ID: NCT03016273

Last Updated: 2017-07-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-20

Study Completion Date

2018-03-31

Brief Summary

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Cesarean section is a surgical procedure used to deliver one or more babies. cesarean section is usually performed when vaginal delivery will put the mother or child's health or life at risk. In recent years, the number of cesarean section has risen worldwide.

Detailed Description

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Conditions

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Cesarean Delivery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

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Bladder flap

The bladder flap is made by superficially incising and dissecting the peritoneal lining to separate the urinary bladder from the lower uterine segment.

Group Type EXPERIMENTAL

creation of bladder flap

Intervention Type PROCEDURE

Creation of the bladder flap, i.e., dissecting the urinary bladder from the lower segment of the uterus is a standard part of cesarean section (CS).

Non bladder flap

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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creation of bladder flap

Creation of the bladder flap, i.e., dissecting the urinary bladder from the lower segment of the uterus is a standard part of cesarean section (CS).

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Patients undergoing elective primary cesarean section
2. previous cesarean section
3. gestational age 32 or more.

Exclusion Criteria

1. Patients undergoing emergent cesarean section
2. Patients undergoing planned vertical uterine incision.
3. Patients undergone previous laparotomies.
4. Gestational age less than 32 weeks .
5. Patient refusing to participate in the study
6. Women with body mass index \>35
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Yasmin mohamed Alaa eldin mahmoud Youssef

Dr

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Assuit university

Asyut, , Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Yasmin Youssef, MBBCh

Role: CONTACT

00201068248305

Tarek A. Farghaly, PHD

Role: CONTACT

+20100 1338099

Facility Contacts

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Ahmed Abbas

Role: primary

Other Identifiers

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BFCS

Identifier Type: -

Identifier Source: org_study_id

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