Effect of Wet Cupping on Blood Components of Healthy volunteers
Phase 3
- Conditions
- Healthy condition.
- Registration Number
- IRCT2014121620329N1
- Lead Sponsor
- Investigator
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 20
Inclusion Criteria
Healthy male 20-70 years old volunteers, who come to traditional medicine clinic for routine annual wet cupping.
Exclusion criteria: Chronic disease patients and patients under medication
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Metobonomics of venous blood and cupping blood. Timepoint: On the same day before and after cupping, 2 weeks later. Method of measurement: Using 1H Nuclear Magnetic Resonance by NMR apparatus.
- Secondary Outcome Measures
Name Time Method Triglyceride. Timepoint: On the same day between venous blood and cupping blood , 2 weeks later between first and second venous blood. Method of measurement: With the use of biochemical kits (Pars Azmoon) and autoanalyzer RA 1000.;High density lipoprotein (HDL). Timepoint: On the same day before and after cupping, 2 weeks later. Method of measurement: Using biochemical kits (Pars Azmoon) and autoanalyzer RA 1000.;Low density lipo proteins (LDL). Timepoint: On the same day before and after cupping, 2 weeks later. Method of measurement: Using biochemical kits(Pars Azmoon) and autoanalyzer RA 1000.;Uric acid. Timepoint: On the same day before and after cupping, 2 weeks later. Method of measurement: Using biochemical kits (Pars Azmoon) and autoanalyzer RA 1000.;Liver enzymes. Timepoint: On the same day before and after cupping, 2 weeks later. Method of measurement: Using biochemical kits (Pars Azmoon) and autoanalyzer RA 1000.