Skip to main content
Clinical Trials/IRCT20161208031300N1
IRCT20161208031300N1
Completed
Phase 3

Study of the effect of resistance training and nano curcumin supplementation on synovial fluid biomarkers in patients with knee osteoarthritis.

Bojnourd University of Medical Sciences0 sites60 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Bojnourd University of Medical Sciences
Enrollment
60
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Bojnourd University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Having an OA (primary) knee with a grade of 1 to 4
  • Low mobility (Participate in sports activities less than three times a week for less than 20 minutes during the past six months and lack of participation in organized activities over the past year)
  • The age range is between 45\-60 years
  • Non\-acute illness like cardiovascular disease and lack of fracture and injury In the lower extremity or a joint infection
  • Lack of endocrine and metabolic diseases (diabetes, thyroid, kidney, liver), cardiovascular disease (high blood pressure, coronary artery disease and atherosclerosis, peripheral vascular diseases and myocardial infarction), mental illness (depression, Schizophrenia and mania), epilepsy, anemia, cancer and any infectious disease.
  • No history of alcohol and smoking and any addiction

Exclusion Criteria

  • Unwillingness of patients to continue cooperation in research
  • No synovial fluid during aspiration
  • Knee joint limitation and inability to perform sports exercises
  • Any injuries when doing exercises
  • Taking medications other than diclofenac for the treatment of osteoarthritis
  • Suffering from cardiovascular, liver, diabetes, kidney failure
  • Age range less than 45 and more than 60 years
  • Addiction and alcohol and smoking
  • Joint infection

Outcomes

Primary Outcomes

Not specified

Similar Trials