Lumbar Radiculopathy Clinical Trial
Official title:
Experimental-controlled, Randomized, Single Blind Trial of Effectiveness of Positional Distraction With Stabilization Exercises Versus Stabilization Exercises Alone in the Management of Lumbar Radiculopathy.
NCT number | NCT04427423 |
Other study ID # | SKhan |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 10, 2020 |
Est. completion date | January 25, 2021 |
Verified date | February 2021 |
Source | Dow University of Health Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluate the addition of positional distraction to stabilization exercises in the treatment of lumbar radiculopathy in adults. Half of the patients will recieve positional distraction and stabilization exercises in combination, while the other half will recieve stabilization exercises only.
Status | Completed |
Enrollment | 96 |
Est. completion date | January 25, 2021 |
Est. primary completion date | December 12, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 50 Years |
Eligibility | Inclusion Criteria: - Clinical diagnosis of lumbar radiculopathy - Age limit 30-50 years - Both males and females - Pain history more than 12 weeks but less than one year - Patient having lumbar disc bulge at maximum two adjacent levels Exclusion Criteria: - Any type of tumor and infection in the spine - Spondylolisthesis at L4- L5, L5-S1 - Fracture of the lumbar spine - Sciatica other than lumbar region (piriformis syndrome) - Acute cardiopulmonary conditions - Morbid obesity (BMI > 30) |
Country | Name | City | State |
---|---|---|---|
Pakistan | Dow University of Health Sciences | Karachi | Sindh |
Lead Sponsor | Collaborator |
---|---|
Dow University of Health Sciences |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline Pain intensity at 8 weeks | The pain intensity measured on self reported Visual Analogue Scale. (0 means no pain and 10 is the high intensity of pain). | All the subjects were assessed before and after 8 weeks of treatment. | |
Primary | Change from baseline Disability at 8 weeks | The disability were assessed on Roland Morris Disability Questionnaire. where 0 means no disability and 24 is the high disability. | All the subjects were assessed before and after 8 weeks of treatment. |
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