Transobturator Paravaginal Repair
ProcedureTransobturator application of sutures to the white line in cases needing paravaginal repair
NCT Number: NCT03489902
Clinical trial comparing the new technique for paravaginal repair versus the traditional technique
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Notify Me20 year–50 year
Female
Interventional
Not applicable
trial comparing the transobturator paravaginal repair versus the traditional technique
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
Transobturator application of sutures to the white line in cases needing paravaginal repair
traditional transvaginal application of sutures to the white line
Time frame: 1 day
Operative time
Time frame: 3 month
Evaluation of the postoperative degree of anterior vaginal wall descent
Time frame: 1 day
blood loss
Ain Shams Maternity Hospital
Other
Transvaginal Versus Transobturator Paravaginal Repair Trial
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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.
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