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Physiotherapy and Capsulitis

Not Applicable
Terminated
Conditions
Arthritis
Registration Number
NCT01789463
Lead Sponsor
Hopital Foch
Brief Summary

Multicenter randomised study, on parallel groups to compare recovery of functional amplitude following shoulder dilatation with auto rehabilitation in one group and physiotherapy in the other group.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • Primary idiopathic phase 2 capsulitis
  • Diagnosis of capsulitis confirmed by shoulder dilatation
  • Patients between 18 and 70 years of age
Exclusion Criteria
  • Secondary capsulitis
  • Shoulder pain of other etiology
  • Cognitive disorders
  • Patients less than 18 years, and more than 70 years of age

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Function of the shoulder joint (Score de Constant)12 months post shoulder dilatation
Secondary Outcome Measures
NameTimeMethod
Pain Visual Analogue Scale (at evening, rest, and at movement)12 months post shoulder dilatation

Trial Locations

Locations (1)

Hôpital FOCH

🇫🇷

Suresnes, France

Hôpital FOCH
🇫🇷Suresnes, France

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