Effectiveness of Shock Wave Therapy Versus Low Level Lazer Therapy in Diabetic Frozen Shoulder Patients.

Diabetes Complications Clinical Trial

Official title:

Effectiveness of Shock Wave Therapy Versus Low Level Lazer Therapy in Diabetic

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05967923
• Other study ID #: P.T- ORTH-06/2023-516
• Status: Recruiting
• Phase: N/A
• Start date: July 5, 2023
• Est. completion date: November 15, 2024

Study information

• Verified date: July 2023
• Source: South Valley University
• Contact: Shymaa Yussuf Abo zaid
• Phone: 01010941685
• Email: shaymaayoussef397[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Patients will be divided randomly into 3 groups.

Description:

Patients will be allocated from out patient clinics of Qena university hospitals Then they will be randomly assigned to three groups, every one will contain 30 patients of both gender, with age range between 45 and 60 years old

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: November 15, 2024
• Est. primary completion date: October 15, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years to 60 Years

Eligibility

Inclusion Criteria:

• patients with diabetes mellitus.

• patients with frozen shoulder due to diabetes mellitus.

• patients age ranged between 45 and 60 years old.

• cooperative patients.

Exclusion Criteria:

• patients with un-controlled hypertension.

• patients sensetive to shock wave or lazer irradiation.

• Patients with infectious skin diseases.

• un-cooperative patients.

Related Conditions & MeSH terms

• Diabetes Complications

Intervention

Radiation:
• Shock wave therapy
Patients in this group will receive shock wave therapy once a week for four weeks in addition to routine physical therapy program.
• Low level lazer therapy
Patients in this group will receive low level lazer therapy three times a week week for four weeks in addition to routine physical therapy program.

Other:
• Routine physical therapy program
Patients in this group will receive only routine physical therapy program three times a week for four weeks.

Locations

Country	Name	City	State
Egypt	Shymaa yussuf abo zaid	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
South Valley University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Shoulder joint Pain	By using visual analogue scale	4 weeks
Primary	Range of motion of the shoulder	Range of shoulder internal and external rotation and shoulder flexion	4 weeks
Secondary	Shoulder and hand disability	By using quick DASH questionnaire	4 weeks