Rectal Prolapse
Conditions
Keywords
ventral rectopexy, biological mesh
Brief 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).
Interventions
DEVICECELLIS Rectopexy (Porcine Acellular Dermal Matrix, PADM)
Biological membrane used in Laparoscopic Ventral Rectopexy (LVR) or robotic assisted rectopexy
Sponsors
Meccellis Biotech
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient aged ≥18 years, * Patient with an indication of rectal prolapse repair by ventral rectopexy (external and internal rectal prolapse), * Patient being informed of its participation to the study and of the follow-up visits, and having no objection to the clinical data collection and medical file access, * Patient being informed of the porcine origin of the device in advance of the procedure.
Exclusion criteria
* Patient with known hypersensitivity to porcine materials, * Patient with an existing infection not appropriately treated, * Patient who are pregnant, * Patient having refused to participate to the study, * Patient refusing to come back to the follow-up visits.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of adverse events including reoperation and removal of the mesh | From the surgical procedure through the entire 24-month follow-up period | Percentage |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Rate of structural defect recurrence requiring reoperation | Throughout the study until end of the 24-month follow-up period | Percentage |
| Symptoms evolution: presence or absence of symptoms (constipation, fecal incontinence, bloody and/or mucous rectal discharge (soiling), unsatisfactory sexual activity, pain) | At baseline and at 30-day, 6-month, 12-month and 24-month follow-up visits | Described at each visit and compared to baseline |
| Symptoms severity scored by a visual analog scale (0-10; 0 corresponding to no impact on life and 10 corresponding to extreme, incapacitating impact) | At baseline and at 30-day, 6-month, 12-month and 24-month follow-up visits | Described at each visit and compared to baseline |
| Rate of symptoms recurrence | Throughout the study until end of the 24-month follow-up period | Percentage |
| Rate of structural defect recurrence based on rectal examination with/without adjunctive investigations as clinically indicated | Throughout the study until end of the 24-month follow-up period | Percentage |
| Severity of disease by the use of the Obstructed Defecation Score (ODS) | At baseline and at 30-day, 6-month, 12-month and 24-month follow-up visits | Change from screening of total score at each follow-up visit. The ODS score is the sum of all points, with a minimum of 0 point and a maximum possible of 31 points with higher scores meaning worse outcome. |
| Quality of life by the use of the Short Form (36) Health Survey (SF-36) questionnaire | At baseline and at 24-month | Change from screening of each domain score and total score at 24-month. The SF-36 has eight scaled scores; the scores are weighted sums of the questions in each section. Scores range from 0 - 100 with lower scores = more disability, and higher scores = less disability |
| Description of device deficiency: inadequacy of a medical device with respect to its identity, quality, durability, reliability, safety or performance. Device deficiencies include malfunctions, use errors, and inadequate labelling. | During the surgical procedure | Summarized and listed |
| Severity of disease by the use of the Cleveland Clinic Incontinence Score (CCIS) | At baseline and at 30-day, 6-month, 12-month and 24-month follow-up visits | Change from screening of total score at each follow-up visit. This scoring system cross-tabulates frequencies and different anal incontinence presentations (Gas/Liquid/Solid/Pad use/Need for lifestyle alterations) and sums the returned score to a total of 0-20 (where 0 = perfect continence and 20 = complete incontinence). |
Countries
France
Outcome results
None listed