Completed PHASE4 INTERVENTIONAL 2-arm NCT00153231

Posterior IVS Versus Sacrospinous Suspension in Vaginal Vault Prolapse Repair

Clinical Evaluation of Morbidity and Efficacy of Posterior IVS (Infracoccygeal Sacropexy), in Comparison to the Standard Sacrospinous Suspension in the Surgical Treatment of Vaginal Vault Prolapse by the Vaginal Route.

Sponsor: Centre Hospitalier Universitaire de Nīmes

Conditions Vaginal Prolapse

Interventions IVS Sacrospinofixation

Updated 6 times since 2017 Last updated: Mar 26, 2015 Started: Mar 31, 2003 Primary completion: Dec 31, 2005 Completion: May 31, 2007

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE4 trial investigates Vaginal Prolapse and is currently completed. Centre Hospitalier Universitaire de Nīmes leads this study, which shows 6 recorded versions since 2003 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

Change History

6 versions recorded

Sep 2025 — Present [monthly]

Completed PHASE4
Sep 2024 — Sep 2025 [monthly]

Completed PHASE4
Jul 2024 — Sep 2024 [monthly]

Completed PHASE4
Jan 2021 — Jul 2024 [monthly]

Completed PHASE4
Jun 2018 — Jan 2021 [monthly]

Completed PHASE4

▶ Show 1 earlier version

Jan 2017 — Jun 2018 [monthly]

Completed PHASE4

First recorded

Mar 2003

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Centre Hospitalier Universitaire de Nīmes

Data source: Centre Hospitalier Universitaire de Nīmes

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Nîmes, France