Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05235854

Six-month Performance of Meniscal Wall Infiltration Under Ultrasound to Treat Stable Degenerative Meniscal Injuries.

Evaluation of the Performance of Six-month Wall Infiltration Under Ultrasound to Treat Stable Degenerative Meniscal Injuries. A Single-center, Randomized, Double-blind Study.

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Centre Hospitalier Universitaire de Nīmes · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main hypothesis of the study is that in situ infiltration of the meniscal lesion would provide patients with lasting and greater relief than intra-articular infiltration. A statistically significant difference would be if the Lysholm score of the meniscal wall group at 3 months is 9.5 points higher than that of the intra-articular infiltration group. The aim is to evaluate the effectiveness of meniscal wall infiltration under ultrasound in the treatment of stable degenerative meniscal lesions versus intra-articular infiltration (Gold standard) at 3 months by Lysholm's algo-functional score.

Conditions

Interventions

TypeNameDescription
DRUGInjection of corticosteroids (Diprostène®)Diprostène® will be injected into the knee. This is a 1 ml syringe of Betamethasone 2 mg, suspension for injection in pre-filled syringe.

Timeline

Start date
2022-05-12
Primary completion
2025-08-01
Completion
2025-11-01
First posted
2022-02-11
Last updated
2024-05-17

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05235854. Inclusion in this directory is not an endorsement.