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Clinical Trial Summary

The purpose of the study is to describe the rate of bone fusion (radiological consolidation) in the 2 groups (A and B) 4 months after the operation.


Clinical Trial Description

The main objective of the study is to describe the rate of bone fusion obtained with the different types of osteosynthesis material: dorsal plate, large-diameter compression screw. Patients will be divided into two groups: - patient undergoing arthrodesis of the hallux with a large diameter screw (group A) - patient undergoing arthrodesis of the hallux by plate (group B) This is a prospective, cross-sectional, open, comparative, non-randomized, non-interventional, monocentric study on two methods of synthesis (large-diameter plate or screw) of hallux metatarsophalangeal arthrodesis. Patients will be managed in accordance with current practice, the choice of surgical strategy (percutaneous / open) being left to the discretion of the investigators. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05691075
Study type Observational
Source GCS Ramsay Santé pour l'Enseignement et la Recherche
Contact Julien BELDAME, MD
Phone 276203095
Email julien.beldame@gmail.com
Status Recruiting
Phase
Start date March 15, 2023
Completion date June 2025

See also
  Status Clinical Trial Phase
Completed NCT04468555 - Hallux Valgus Manual Therapy Based on Global Postural Reeducation. N/A
Completed NCT05258695 - The Turkish Version of the AOFAS Hallux MTP-IP