An interventional study of Sheep Tail Fat and Standard medical treatment in Gonarthrosis, sponsored by Inonu University. Recruiting at 2 sites in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-09.
Sponsored by Inonu University · Not applicable, Interventional, and Supportive care
In recent years, experimental and clinical studies conducted on sheep tail fat, a natural and easily accessible resource, have shown that bioactive components found in sheep tail fat, such as palmitic acid, stearic acid, oleic acid, linoleic acid, and myristic acid, have anti-inflammatory and chondroprotective (cartilage-protective) properties. In addition, literature reviews have revealed that sheep tail fat alleviates joint pain and has a positive effect on joint stiffness. Sheep tail fat is known to be frequently used by patients with gonarthrosis (knee osteoarthritis) in Türkiye and many other countries as a traditional and complementary medicine method.
In this context, this study is designed as a randomized controlled experimental study to evaluate the effects of sheep tail fat application on pain, joint stiffness, and activities of daily living in patients with gonarthrosis. The study population consists of patients diagnosed with gonarthrosis who apply to the Physical Therapy and Rehabilitation outpatient clinics of two state hospitals located in Bitlis. According to the sample size calculation performed using G*Power 3.1.9.7 software, a total of 66 participants were determined and randomly assigned to the experimental and control groups. Participants in the experimental group will receive topical sheep tail fat application in addition to standard medical treatment, while the control group will continue to receive standard medical treatment only.
Data collection tools include the Patient Identification Form developed by the researcher, the Visual Analog Scale (VAS) for assessing pain intensity, and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) for assessing pain, joint stiffness, and daily physical function. These scales will be administered at baseline and again after completion of the intervention period.
The double-boiler (bain-marie) method is used to obtain the sheep tail fat, and participants are provided with training on the application techniques. The required ethics committee approval and institutional permissions from the relevant healthcare institutions have been obtained, and written informed consent has been obtained from all participants. Hamdani sheep, one of the sheep breeds commonly raised and traditionally preferred in the region where the study is conducted, are used to obtain the sheep tail fat.
For the statistical analysis of the data, in addition to descriptive statistics, the paired-samples t-test or Wilcoxon signed-rank test will be used for within-group comparisons, while the independent-samples t-test or Mann-Whitney U test will be used for between-group comparisons. When the assumptions of parametric tests are not met, appropriate non-parametric methods will be preferred.
This study aims to contribute scientifically to clinical decision-making processes regarding traditional and complementary treatment approaches by evaluating, within an evidence-based framework, the effectiveness of a method traditionally used for the management of gonarthrosis symptoms in many countries. It also aims to support the standardization of traditional, complementary, and alternative medicine practices and to provide scientific evidence regarding a low-cost, natural, non-invasive, and accessible alternative treatment option. In addition, the findings are expected to guide the development of new strategies to improve functional well-being in patients with gonarthrosis.
3,391 studies on the registry are indexed under Osteoarthritis, Knee; 628 are open to participants now.
This study's planned enrollment of 66 is close to the median of 69 across 2,808 interventional studies indexed under Osteoarthritis, Knee.
Browse Osteoarthritis, Knee studies →Inonu University is the lead sponsor of 384 studies on the registry; 90 are open to participants now.
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**Inclusion Criteria**
**Exclusion Criteria**
Participants in this group will receive topical sheep tail fat application in addition to standard medical treatment.
Other: Sheep Tail Fat
Participants in this group will receive standard medical treatment only.
Other: Standard medical treatment
Topical application of sheep tail fat to the knee once daily for two weeks, seven days per week, with each application lasting at least three hours.
Participants in the control group will receive standard medical treatment only.
Pain intensity measured by the Visual Analog Scale (VAS)
Pain intensity will be assessed using the Visual Analog Scale (VAS), ranging from 0 to 10, with higher scores indicating greater pain intensity.
Time frame: Baseline and 2 weeks
Plan to share: No
No publications or documents are linked to this record.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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