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Trials / Completed

CompletedNCT04130555

Safety and Performance Evaluation of a Biological Matrix Used for Rectal Prolapse Repair by Ventral Rectopexy

Observational Prospective Study of a Non-cross-linked Porcine Acellular Dermal Matrix in Ventral Mesh Rectopexy

Status
Completed
Phase
Study type
Observational
Enrollment
55 (actual)
Sponsor
Meccellis Biotech · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The general objective of the study is to confirm the medium/long-term safety and clinical performance of the CELLIS Rectopexy membrane used in rectal prolapse repair by ventral rectopexy and to identify emerging risks in comparison to the clinical data related to other types of fixation material. The present study will be a prospective multicentric non-randomized and non-controlled trial involving 55 patients followed for 24 months. The study will be conducted in France in 3 investigational centres.

Detailed description

The study will be prospective, multicentric, single-arm, observational (non-interventional) to evaluate the safety and performance of CELLIS Rectopexy used in rectal prolapse repair by ventral rectopexy. All evaluations will be performed and products used according to the usual practice, without additional or unusual diagnostic, treatment and monitoring procedure. The study will be conducted in France in 3 investigational centres including 55 patients scheduled for the repair of rectal prolapse. Each patient will participate in one assessment period including a screening visit, followed by the day of surgical procedure and a hospitalization period. Patients will return for ambulatory visits at Day 30 (+/- 7 days), Month 6 (+/- 2 weeks), Month 12 (+/- 2 weeks) and Month 24 (+/-2 weeks). The surgical technique used to repair rectal prolapse will be either Laparoscopic Ventral Rectopexy (LVR) or a robotic assisted rectopexy with the use of the da Vinci Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA).

Conditions

Interventions

TypeNameDescription
DEVICECELLIS Rectopexy (Porcine Acellular Dermal Matrix, PADM)Biological membrane used in Laparoscopic Ventral Rectopexy (LVR) or robotic assisted rectopexy

Timeline

Start date
2019-12-11
Primary completion
2023-10-26
Completion
2023-10-26
First posted
2019-10-17
Last updated
2023-10-27

Locations

3 sites across 1 country: France

Source: ClinicalTrials.gov record NCT04130555. Inclusion in this directory is not an endorsement.

Safety and Performance Evaluation of a Biological Matrix Used for Rectal Prolapse Repair by Ventral Rectopexy (NCT04130555) · Clinical Trials Directory