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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03850249
Other study ID # RECHMPL19_0010
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date May 31, 2018

Study information

Verified date December 2020
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators conduced a clinical trial to evaluate the clinical and radiographic results after radioscapholunate fusion in case of posttraumatic radiocarpal osteoarthritis. Because of poor clinical result, many authors upgrade the procedure including excision of the distal pole of the scaphoid and later excision of the entire triquetrum. Only one study compared the three procedures in 17 patients. The investigators performed the same comparison in 85 patients with a mean follow up of 9,1 years (1-23)


Description:

The investigators compared three populations: patients with radioscapholunate (RSL) fusion alone, patients with RSLfusion and distal scaphoid excision and patient with RSL fusion, distal scaphoid excision and excision of the triquetrum. The investigators performed clinical (pain, grasp strength, wrist motion), functional and radiographic (midcarpal osteoarthritis and radiocarpal nonunions) evaluation


Recruitment information / eligibility

Status Completed
Enrollment 85
Est. completion date May 31, 2018
Est. primary completion date May 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - posttraumatic radiocarpal osteoarthritis - Patients who underwent radioscapholunate fusion Exclusion criteria: - Patients with radiocarpal osteoarthritis due to rheumatoid or inflammatory disease and Kienböck disease - Patients with posttraumatic radiocarpal osteoarthritis managed with other surgery

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Montpellier Nancy University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary presence of mediocarpal osteoarthritis To evaluate the long-term radiographic results of post-traumatic radio scapholunate 1 day
Primary presence of scapho-trapezoidal trapezoid To evaluate the long-term radiographic results of post-traumatic radio scapholunate 1 day
Primary presence of non-consolidation of radio-scapho-lunar arthrodesis To evaluate the long-term radiographic results of post-traumatic radio scapholunate 1 day
Secondary Assess overall survival To evaluate the overall survival (excluding total wrist arthrodesis) of post-traumatic radio scapholunate 1 day
Secondary the prognostic factors of good clinical To evaluate the prognostic factors of good clinical (ie absence of osteoarthritis or good consolidation of arthrodesis) 1 day
Secondary the prognostic factors of radiographic evolution To evaluate the prognostic factors of radiographic evolution (ie absence of osteoarthritis or good consolidation of arthrodesis) 1 day