# A Study Evaluating the Clinical Outcome of a Modified d'Hoore Technique for Laparoscopic Ventral Mesh Rectopexy

> **NCT04564677** · — · UNKNOWN · sponsor: **Duomed** · enrollment: 150 (estimated)

## Conditions studied

- Rectocele
- Enterocele
- Rectal Prolapse

## Interventions

- **DEVICE:** Ifabond (Péters surgical)

## Key facts

- **NCT ID:** NCT04564677
- **Lead sponsor:** Duomed
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2021-02-08
- **Primary completion:** 2025-11-30
- **Final completion:** 2025-12-31
- **Target enrollment:** 150 (ESTIMATED)
- **Last updated:** 2023-10-10


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04564677

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04564677, "A Study Evaluating the Clinical Outcome of a Modified d'Hoore Technique for Laparoscopic Ventral Mesh Rectopexy". Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/clinical/NCT04564677. Licensed CC0.

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