# Pelvic Floor Repair Systems for Prolapse Repair

> **NCT00638235** · — · COMPLETED · sponsor: **ASTORA Women's Health** · enrollment: 725 (actual)

## Conditions studied

- Pelvic Organ Prolapse

## Interventions

- **DEVICE:** AMS Apogee™ with IntePro
- **DEVICE:** AMS Apogee™ with Intexen LP
- **DEVICE:** AMS Perigee™ with IntePro
- **DEVICE:** AMS Perigee™ with IntePro Lite
- **DEVICE:** AMS Apogee™ with IntePro Lite
- **DEVICE:** AMS Elevate™ Apical & Posteiror with IntePro Lite
- **DEVICE:** AMS Elevate™ Apical & Posteiror with IntXen LP
- **DEVICE:** AMS Elevate™ Anterior & Apical with IntePro Lite (Gen 1, For Study Use Only)
- **DEVICE:** AMS Elevate™ Anterior & Apical with IntePro Lite (Gen 2)

## Key facts

- **NCT ID:** NCT00638235
- **Lead sponsor:** ASTORA Women's Health
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2006-05
- **Primary completion:** 2011-02
- **Final completion:** 2012-09
- **Target enrollment:** 725 (ACTUAL)
- **Last updated:** 2016-10-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00638235

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00638235, "Pelvic Floor Repair Systems for Prolapse Repair". Retrieved via MORVS 2026-10-10 from https://api.morvs.ai/clinical/NCT00638235. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*