The Effect of Tail Fat Application on Joint Pain, Joint Stiffness, and Daily Living Activities in Patients With Gonarthrosis
- NCT ID
- NCT07867405
- Registry status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- Inonu University
- Conditions
- Gonarthrosis
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 66 participants (Estimated).
What is being studied
- Other: Sheep Tail Fat
- Other: Standard medical treatment
Who may be eligible
- Ages
- 18 Years to no maximum
- Sex
- All
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
\*\*Inclusion Criteria\*\*
* Patients diagnosed with gonarthrosis by a physician.
* Patients with a VAS score above 4.
* Individuals who have experienced pain related to knee osteoarthritis for at least the last 3 months.
* Participants aged 18 years and older.
* Individuals without an allergy to sheep tail fat or other animal products.
* Individuals who can communicate in Turkish and understand written and verbal instructions.
* Individuals who can apply the sheep tail fat according to the instructions.
* Individuals who agree to participate in the study.
\*\*Exclusion Criteria\*\*
* Individuals with severe physical disability or mental/psychological problems in the knee region.
* Individuals with intellectual or cognitive limitations.
* Individuals who have undergone knee surgery within the last year.
* Individuals with peripheral vascular disease.
* Individuals with infection, wound, cellulitis, or active skin disease in the knee region.
* Individuals who have experienced knee trauma or received an intra-articular steroid injection within the last six months.
* Individuals diagnosed with secondary arthritis or inflammatory joint disease.
* Pregnant or breastfeeding women.
* Individuals with active bleeding disorders.
* Individuals with asthma and individuals with liver or kidney failure.
* Individuals with connective tissue diseases (e.g., lupus, systemic sclerosis).
* Individuals who have experienced a serious infection within the last three months or are immunosuppressed.
* Individuals with neurological diseases affecting knee stability.
Study locations
2 study locations are listed.
Recruiting site status is explicitly provided for 2 locations; 2 are listed as Recruiting.
Countries: Turkey (Türkiye)
Sample of listed locations
- Bitlis State Hospital — Bitlis, Turkey (Türkiye) — Recruiting
- Bitlis Tatvan State Hospital — Bitlis, Turkey (Türkiye) — Recruiting
Study details
- Start date
- May 12, 2026
- Primary completion date
- January 31, 2027
- Completion date
- January 31, 2027
- First posted
- October 9, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07867405
- Registry last updated
- October 9, 2026
- QualifiedStudies registry data refreshed
- October 12, 2026
- QualifiedStudies record fetched
- October 12, 2026
View NCT07867405 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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