Comparing Kaltenborn and Mulligan techniques for treating Carpal Tunnel Syndrome
Comparative Effects of Kaltenborn Versus Mulligan Mobilisation on Pain, Disability and Hand Function in Patients With Carpal Tunnel Syndrome
This study is testing whether two different hands-on therapy techniques can help people with Carpal Tunnel Syndrome feel less pain and improve their hand function.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 48 (estimated) |
| Ages | 20 Years to 45 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab Province) |
| Trial ID | NCT06687018 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of two manual therapy techniques, Kaltenborn and Mulligan mobilization, in alleviating pain, disability, and improving hand function in patients diagnosed with Carpal Tunnel Syndrome (CTS). The study will involve 48 participants aged 20 to 45 who exhibit symptoms such as pain, tingling, and numbness in the median nerve distribution. Participants will be randomly assigned to one of two groups, each receiving a different mobilization technique over a period of six weeks. Outcomes will be measured using standardized questionnaires to assess pain levels, disability, and hand function.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 20 to 45 experiencing localized pain, tingling, and numbness in the median nerve distribution.
Not a fit: Patients with sensory or motor deficits in other nerves, previous hand surgeries, or systemic diseases like diabetes or rheumatoid arthritis may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective non-surgical treatment options for patients suffering from Carpal Tunnel Syndrome.
How similar studies have performed: Previous studies have shown positive outcomes with manual therapy techniques for similar conditions, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Both genders between 20 and 45 years of age * Individuals having localized pain, tingling and numbness in the median nerve distribution * Positive Tinel sign and positive Phalen's test Exclusion Criteria: * Any sensory and/or motor deficit in either the ulnar or radial nerve traumatic neck injury * Previous hand surgery or trauma or cervical radiculopathy * Systemic disease e.g. diabetes mellitus or thyroid disease or rheumatoid arthritis
Where this trial is running
Lahore, Punjab Province
- Ejaz Hospital — Lahore, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Ali Raza, MS-OMPT — Riphah International University
- Study coordinator: Imran Amjad, Phd
- Email: Imran.amjad@riphah.edu.pk
- Phone: 03324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.