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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05905107
Other study ID # REC_FSD_00325
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 4, 2023
Est. completion date July 30, 2023

Study information

Verified date June 2023
Source Riphah International University
Contact Sahreen Anwar, Ph.D
Phone +923346591705
Email sahreenanwar@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Carpal tunnel syndrome is a compressive neuropathy of median nerve in the fascial tunnel at wrist which causes pain, numbness ,and tingling in the extremities. Common treatment options used in the treatment of carpal tunnel syndrome are conservative and surgical treatment option is better, this question is still a topic requiring more and more clinical trials. Neuromobilisation described by Butler is one of the treatment options which are used in the treatment of carpal tunnel syndrome in conjunction with other conservative measures. This proposed study will find out the effectiveness of Neuromobilisation in treatment of carpal tunnel syndrome. As there is very little evidence available which Neuromobilisation technique is effective and what are the types of patients which can get benefit from this technique. This study will find out the effect of Neuromobilisation in patients suffering from carpal tunnel syndrome of non traumatic origin. This is a randomized clinical trial. Target population is patients suffering from carpal tunnel syndrome of non-traumatic origin. Data will be collected from District Headquarter Hospital Faisalabad. This study will include 56 participants according to the selection criteria. The participants will be randomly divided into two groups through sealed opaque envelop method. Group A will recruit 28 patients which fulfill the inclusion criteria. These patients will be treated by nerve sequencing proximal to distal in 3 sets of 15 repetitions in one session on alternate days for 4 weeks. Group B will recruit 28 patients which fulfill the inclusion criteria. These patients will be treated by nerve sequencing distal to proximal in 3 sets of 10 repetitions in one session for 4 weeks. The Statistical analysis will be performed through SPSS Software 21.


Recruitment information / eligibility

Status Recruiting
Enrollment 56
Est. completion date July 30, 2023
Est. primary completion date July 15, 2023
Accepts healthy volunteers No
Gender All
Age group 25 Years to 55 Years
Eligibility Inclusion Criteria: - Patients positive for provocative test ( Phalen's test, Wrist decompression test and tinnel test). Exclusion Criteria: - Inflammation around the wrist - Tumor around the wrist - Rheumatoid Arthritis - Osteoporosis - Joint Hypermobility

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Neurodynamic Slider Technique from Proximal to Distal
Neurodynamic Slider Technique from proximal to distal at wrist, elbow and neck
Neurodynamic Slider Technique from Distal to Proximal
Neurodynamic Slider Technique from proximal to distal at wrist, elbow and neck

Locations

Country Name City State
Pakistan District Headquarters Hospital Faisalabad Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain at wrist joint Pain will be assessed by using Numerical Pain Rating Scale Pain will be assessed by using Numerical Pain Rating Scale 4 weeks
Primary Wrist Range of Movement at wrist joint Range of motion will be assessed by using Goniometer 4 weeks
Primary Functional Ability at wrist joint Functional Ability will be assessed by using Boston Carpal tunnel syndrome 4 weeks
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