Frozen Shoulder Clinical Trials

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Investigation of the Effectiveness of Exercise and Anti-Fibrotic Approaches in Frozen Shoulder

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this clinical study is to investigate the efficacy of losartan as an antifibrotic approach in addition to a physiotherapy program in patients diagnosed with frozen shoulder. The effects of losartan use on pain intensity, shoulder joint range of motion, functional status, and pain catastrophizing level will be evaluated and compared with the outcomes of patients participating in a physiotherapy program alone. The key questions this study aims to answer are: * Is there a difference in shoulder functionality between frozen shoulder patients using losartan in addition to a physiotherapy program and those participating in a physiotherapy program alone? * Is there a difference in pain intensity, shoulder joint range of motion, and pain catastrophizing level between frozen shoulder patients using losartan in addition to a physiotherapy program and those participating in a physiotherapy program alone? A total of 33 patients will be enrolled in the study. Participants will be randomly assigned to one of two groups: the physiotherapy group (PT) and the physiotherapy + losartan group (PT+L). Both groups will receive the same physiotherapy program comprising range of motion exercises, stretching exercises, strengthening exercises, and mobilization techniques. Patients in the PT+L group will additionally receive 12.5 mg of oral losartan once daily for four weeks. Clinical assessments will be conducted at baseline, at week 4, and at week 8.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults aged 18 years or older diagnosed with frozen shoulder (adhesive capsulitis)

• Having less than 50% of range of motion (ROM) in at least one of the following shoulder movements compared to the unaffected side: external rotation, abduction, flexion, or internal rotation

• Having more than 25% loss of ROM in at least two movement planes compared to the unaffected shoulder

• Patients in stage II or III of frozen shoulder

Locations
Other Locations
Turkey
Istanbul University-Cerrahpasa
RECRUITING
Istanbul
Contact Information
Primary
Ayşe Betül Erol, Bachelor's degree
aysebetul.yildiz@ogr.iuc.edu.tr
+90 534 669 14 06
Time Frame
Start Date: 2026-01-07
Estimated Completion Date: 2027-01
Participants
Target number of participants: 33
Treatments
Active_comparator: Physiotherapy Group (FT)
Participants will receive a physiotherapy program including range of motion exercises, stretching, strengthening exercises, and mobilization techniques. The program will be conducted twice a week for four weeks, totaling eight sessions. During the first session, participants will receive patient education and a home exercise program. After each exercise session, a 15-minute cold application will be applied.
Experimental: Physiotherapy + Losartan Group (FT+L)
Participants will receive the same physiotherapy program as the FT group. In addition, participants in this group will receive 12.5 mg of oral losartan once daily for four weeks.
Related Therapeutic Areas
Sponsors
Leads: Istanbul University

This content was sourced from clinicaltrials.gov