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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