Effects of Spirulina supplementation on ulcerative colitis patients
Not Applicable
- Conditions
- lcerative colitis patients.Ulcerative colitis, unspecifiedK51.9
- Registration Number
- IRCT20191204045612N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Patients with mild to moderate ulcerative colitis in the age range of 18 to 65 years
Exclusion Criteria
Patients with severe ulcerative colitis
Individuals in pregnancy or breastfeeding condition.
Taking antidepressants and anxiety medications.
Taking antioxidant and omega-3 supplements in the last three months.
Smokers or alcohol consumers.
Patients with kidney, liver, thyroid and parathyroid, gastrointestinal and heart disease and cancer disease.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pentraxin 3. Timepoint: Before intervention and 8 weeks after initiation of Spirulina supplementation. Method of measurement: Eliza kit.;Total antioxidant capacity. Timepoint: Before intervention and 8 weeks after initiation of Spirulina supplementation. Method of measurement: Diagnostic kit.;Malondialdehyde. Timepoint: Before intervention and 8 weeks after initiation of Spirulina supplementation. Method of measurement: Diagnostic kit.;Superoxide dismutase. Timepoint: Before intervention and 8 weeks after initiation of Spirulina supplementation. Method of measurement: Diagnostic kit.;Erythrocyte Sedimentation Rate. Timepoint: Before intervention and 8 weeks after initiation of Spirulina supplementation. Method of measurement: Measurement of erythrocyte sedimentation rate.;Disease activity indices. Timepoint: Before intervention and 8 weeks after initiation of Spirulina supplementation. Method of measurement: SCCAI questionnaire.
- Secondary Outcome Measures
Name Time Method