Effect of calcitonin in frozen shoulder treatment

Phase 3

Recruiting

• Conditions: Frozen shoulder.; Adhesive capsulitis of unspecified shoulder; M75.00

• Registration Number: IRCT20220523054971N1
• Lead Sponsor: Islamic Azad University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

Patients with a clinical diagnosis of frozen shoulder
Patients symptoms including limitation in all active and passive movements of the shoulder joint in all directions
Patients with relatively severe pain
Patients with reduction in the range of motion of the shoulder
Definite confirmation of the diagnosis with the help of MRI of the shoulder joint

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain changes with visual analogue scale(VAS). Timepoint: 6 weeks after receiving calcitonin nasal spray. Method of measurement: Visual analogue scale.;Changes in the range of motion with the angle scale in degrees. Timepoint: 6 weeks after receiving calcitonin nasal spray. Method of measurement: Degrees of angle.