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Effects of Spirulina supplementation on ulcerative colitis patients

Not Applicable
Conditions
lcerative colitis patients.
Ulcerative colitis, unspecified
K51.9
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
NameTimeMethod
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
NameTimeMethod
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