Long-term follow up after transvaginal cystocele repair with four-armed collagen-coated mesh

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study looks at long-term safety and effectiveness of transvaginal cystocele repair using a four-armed collagen-coated polyester mesh. It analyzes patients with at least five years of follow-up data to identify durability of the repair and potential late complications. The study focuses on outcomes such as recurrence, mesh-related adverse events, and overall pelvic floor function. Data are gathered from Ain Shams University in Cairo, with inclusion criteria requiring complete follow-up and medical records. Exclusion criteria remove patients with missing data, pelvic radiation/laser/chemotherapy, or uncontrolled diabetes postoperatively.

Why it matters

Who can join: the full rules

Inclusion Criteria:

• Data of patients who underwent transvaginal cystocele repair using four-armed collagen coated polyester mesh

Exclusion Criteria:

* Patients with insufficient postoperative follow-up data.
* Patients with incomplete or missing medical records.
* Patients undergone radiation, laser therapy, or chemotherapy in the pelvic area postoperatively.
* Patients newly discovered uncontrolled diabetes mellitus.

Where it's running

• Ain Shams University
  Cairo, Cairo Governorate, Egypt Recruiting

Study contacts

• Study coordinator: Ibrahem M Abdelghany, MBBCH
• Email: IbrahemAbdelghany@med.asu.edu.eg
• Phone: 00201063256605

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.