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OpenTrials
Completed

NCT Number: NCT03489902

Transvaginal Versus Transobturator Paravaginal Repair

Clinical trial comparing the new technique for paravaginal repair versus the traditional technique

Completed

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Key information

About this study

trial comparing the transobturator paravaginal repair versus the traditional technique

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

paravaginal defect cystocele

midline and paravaginal defect cystocele

Exclusion criteria

  • uterine descent previous cystocele surgery

Treatment and study plan

Transobturator Paravaginal Repair

Procedure

Transobturator application of sutures to the white line in cases needing paravaginal repair

traditional transvaginal Paravaginal Repair

Procedure

traditional transvaginal application of sutures to the white line

Primary outcomes

  1. Operative data

    Time frame: 1 day

    Operative time

Secondary outcomes

  1. Pelvic organ prolapse quantification system

    Time frame: 3 month

    Evaluation of the postoperative degree of anterior vaginal wall descent

  2. Operative Details

    Time frame: 1 day

    blood loss

Sponsors and collaborators

Lead sponsor

Ain Shams Maternity Hospital

Other

Registry information

Official study title

Transvaginal Versus Transobturator Paravaginal Repair Trial

Important dates

Study start
2017
Primary completion
2017
Study completion
2018
First posted
Apr 6, 2018
Registry last updated
Apr 9, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.