# Multi-center Study to Evaluate the Safety and Efficacy of Aesculap MonoMax® for Abdominal Wall Closure

> **NCT00572507** · NA · COMPLETED · sponsor: **Aesculap AG** · enrollment: 150 (actual)

## Conditions studied

- Primary Median Laparotomy

## Interventions

- **DEVICE:** MonoMax®

## Key facts

- **NCT ID:** NCT00572507
- **Lead sponsor:** Aesculap AG
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2007-12
- **Primary completion:** 2008-08
- **Final completion:** 2009-07
- **Target enrollment:** 150 (ACTUAL)
- **Last updated:** 2015-05-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00572507

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00572507, "Multi-center Study to Evaluate the Safety and Efficacy of Aesculap MonoMax® for Abdominal Wall Closure". Retrieved via AI Analytics 2026-07-10 from https://api.ai-analytics.org/clinical/NCT00572507. Licensed CC0.

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