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Effect of punica granatum L . (peel) on ulcerative colitis disease

Phase 2
Conditions
ulcerative colitis.
Noninfective enteritis and colitise
Registration Number
IRCT2014040617156N1
Lead Sponsor
Vice chancellor for research, Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
64
Inclusion Criteria

patients 18 and up to 70 years old; ulcerative colitis identified by clinical criteria, laboratory and endoscopic disease is confirmed; informed consent. Exclusion criteria: addiction; lack of consent to participate or continue to participate in the study; pregnant women; a history of hypersensitivity to the ingredients of pomegranate; taking prednisone above 15 mg daily and / or cyclosporine and / or infleximab.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical features of patients with ulcerative colitis. Timepoint: 4 weeks after intervention. Method of measurement: Lichtiger Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Side effects. Timepoint: 4 weeks after the start of the intervention. Method of measurement: Patient monitoring.
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