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NCT03299114 Clinical Trial

WHIRLPOOL FOR OSTEOARHRITIS

Neuropathic Pain Clinical Trial

Official title:
THE EFFECTIVENESS OF WHIRLPOOL FOR PATIENTS WITH NEUROPATHIC PAIN DUE TO KNEE OSTEOARTHRITIS

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03299114
Other study ID # 30112015-6
Secondary ID
Status Completed
Phase N/A
First received September 27, 2017
Last updated September 27, 2017
Start date November 1, 2015
Est. completion date January 1, 2016

Study information
Verified date September 2017
Source Ufuk University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Both neuropathic and nociceptive mechanisms may contribute to the OA pain experience. Aims: The aim of this study was to determine the efficacy of warm whirlpool on pain, disability, quality of life (QoL) and sleep for patients with neuropathic pain.

Description:

Whirlpool treatment method is used for medical and surgical conditions. In literature there are studies which recommend whirlpool therapy as a treatment for reducing pain in patients with osteoarthritis. The aim of this study was to determine the efficacy of warm whirlpool on pain, disability, quality of life (QoL) and sleep for patients with neuropathic pain.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date January 1, 2016
Est. primary completion date January 1, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 75 Years
Eligibility Inclusion Criteria:

- suffering from knee pain at least 3 months

- radiological manifestations considering were consistent with grade 3 and 4 knee OA due to Kellgren and Lawrence criteria had DN4 scores =4.

Exclusion Criteria:

- lower extremity surgery history, knee infection inflammatory disease like rheumatoid arthritis back or pelvic pain related with knee pain another cause of polyneuropathy (diabetes mellitus, vitamin B 12 deficiency, toxic or neurological disease like stroke, spinal cord injury) lumbar disc herniation malignancy or active systemic disease.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Whirlpool

Locations
Country Name City State
Turkey Ufuk University Ankara

Sponsors (1)
Lead Sponsor Collaborator
Ufuk University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary visual analogue scale one month
Secondary Short Form-36 Health Survey one month
Secondary Western Ontario and McMaster Universities Osteoarthritis Index one month
Secondary Pittsburgh Sleep Quality Index (PSQI) one month
Secondary DN4 one month
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