Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06519058
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-06-27
Brief Title:
Effectiveness of Self-Myofascial Stretching on Carpal Tunnel Syndrome
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Effectiveness of Carpal Ligament Self-Myofascial Stretching Over Conventional Physical Therapy on Reducing Pain and Improving Function in Patients With Stage I and II Carpal Tunnel Syndrome
Status:
COMPLETED
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Background and aim Carpal tunnel syndrome CTS also known as median mononeuropathy occurs when the median nerve is squeezed or compressed as it travels through the carpal tunnel at the wrist The main aim of the study was to compare the effectiveness of carpal ligament self-myofascial stretching over conventional physical therapy on reducing pain and improving function in patients with stage I and II CTS
Methodology Thirty-six subjects with stage I and II CTS who fulfilled the inclusion criteria were randomly assigned to experimental group and control group with 18 patients in each group Experimental Group received carpal ligament self-myofascial stretching along with conventional physical therapy while the Control Group received conventional physical therapy alone The duration of the treatment was 6 weeks The outcome measures used were Boston Carpal Tunnel Questionnaire and Visual Analogue Scale
Methodology Thirty-six subjects with stage I and II CTS who fulfilled the inclusion criteria were randomly assigned to experimental group and control group with 18 patients in each group Experimental Group received carpal ligament self-myofascial stretching along with conventional physical therapy while the Control Group received conventional physical therapy alone The duration of the treatment was 6 weeks The outcome measures used were Boston Carpal Tunnel Questionnaire and Visual Analogue Scale
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None