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Clinical Trial Summary

Monocentric, prospective, randomised, double-blind study of two parallel groups of 66 patients with post-reconstruction ACL hamstring contracture treated with an ultrasound-guided injection at two points on the body of the hamstring - Group 1: botulinum toxin: 100 units (0.5ml) in 1 injection - Group 2: placebo: 0.5 ml in 1 injection


Clinical Trial Description

The study includes three assessments: one month after ligamentoplasty (inclusion visit) and then at M2 and M5. The therapeutic benefit of the study treatments is based on the evolution of the extension defect at M2. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05008731
Study type Interventional
Source GCS Ramsay Santé pour l'Enseignement et la Recherche
Contact Alexandre Hardy, MD
Phone 189164500
Email alexandre.hardy@me.com
Status Not yet recruiting
Phase Phase 3
Start date October 2021
Completion date April 2024

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