Results at More Than 10 Years of Meniscal Sutures Without Avivement
SMI
1 other identifier
observational
100
1 country
1
Brief Summary
Currently, suturing the lesion is recommended rather than the classic meniscectomy, which leads to early and subsequent gonarthrosis. The most commonly practiced technique is arthroscopic suturing after avivement the area to be sutured to promote healing. But the real benefit of this enhancement has never been documented. The complexity of the surgical procedure makes the acceptability of this indication low by orthopedic surgeons at present (10% sutures compared to 90% meniscectomies). The aim of the study is to evaluate the 10-year survival rate of meniscal sutures without avivement.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 8, 2023
CompletedFirst Submitted
Initial submission to the registry
October 18, 2023
CompletedFirst Posted
Study publicly available on registry
October 24, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 8, 2024
CompletedOctober 24, 2023
October 1, 2023
9 months
October 18, 2023
October 18, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
10-year survival rate of meniscal sutures without avivement
10 years after surgery
Eligibility Criteria
Adult patient (≥18 years old) having medial or lateral meniscal lesion of the knee treated by arthroscopic suture without avivement with or without reconstruction of the anterior cruciate ligament and operated on at the HUS between January 1, 2011 and June 30, 2013
You may qualify if:
- Adult patient (≥18 years old)
- Gender indifferent
- Patient operated on at the HUS between January 1, 2011 and June 30, 2013
- Medial or lateral meniscal lesion of the knee treated by arthroscopic suture without sharpening with or without reconstruction of the anterior cruciate ligament.
- Absence of written opposition in the medical file of the subject (and/or their legal representative if applicable) to the reuse of their data for scientific research purposes.
You may not qualify if:
- Subject having expressed his opposition to the reuse of his data for scientific research purposes.
- Subject under judicial protection
- Subject under guardianship or curatorship
- Meniscal lesion not sutured or sutured with sharpening.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service d'Orthopédie - Traumatologie Membre Supérieur - CHU de Strasbourg - France
Strasbourg, 67091, France
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 18, 2023
First Posted
October 24, 2023
Study Start
September 8, 2023
Primary Completion
June 1, 2024
Study Completion
June 8, 2024
Last Updated
October 24, 2023
Record last verified: 2023-10