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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05405647
Other study ID # Cairo Un115
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2021
Est. completion date January 30, 2022

Study information

Verified date June 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study would be conducted to answer the following question: was there any difference between the effects of Shock wave versus Kinesio Tape in the treatment of carpal tunnel syndrome for post-menopausal women.


Description:

Fifty menopausal women with mild to moderate CTS were selected randomly from outpatient clinic of the physical therapy department of El khazendara general hospital, Age was ranged from 45 - 55 years old. Group A, consisted of 25 patients who received a program of 6 session of Shock wave Therapy on the affected wrist,5 minute per session. Group B Represented the control group, it consisted of 25 patients who received a program of kinesio tape application on the affected wrist for 3 days.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date January 30, 2022
Est. primary completion date January 29, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - -Age was ranged from 45 - 55 years old - All subjects would not take analgesics by another route during the study. Exclusion Criteria: - Patients had previous carpal tunnel release. - Skin over sensitivity of some patients to the tape.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Shock wave Therapy
a program of 6 session of Shock wave Therapy on the affected wrist,5 minute per session and a frequency of 5 Hz., 1 sessions per week for 6 weeks.
kinesio tape
kinesio tape application on the affected wrist for 3 days and then one day off and then another 3 days each week for 6weeks.

Locations

Country Name City State
Egypt Ghada Ebrahim Elrefaye Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Computerized electromyography 2 channel version with EMG/NCV/EP system, It was used to measure median motor distal latency (MMDL) before treatment and after 6 weeks of treatment for all patients 6 weeks
Secondary Boston carpal tunnel questionnaire The overall score for the functional-status scale was the mean of the ratings on the 8 daily activities. In this study BCTQ was translated and filled by the therapist 6 weeks
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