Effect of rose oil soft gel on controlling the symptoms of ulcerative colitis
Not Applicable
Recruiting
- Conditions
- ulcerative colitis.Ulcerative colitis
- Registration Number
- IRCT2016120323823N2
- Lead Sponsor
- Shiraz University Of Medical Sciences and barijessence company
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
patients with ulcerative colitis that previously confirmed with colonoscopy ;age> 18-70 years.
exclusion criteria: history of steroid use in the past 4 weeks; history of any NSAIDs use in one week before; history of antibiotic use within 2 weeks before entering the study; any medicinal plants within 2 weeks before entering the study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical symptoms. Timepoint: in at first visit and then weekly during 2 months of treatment. Method of measurement: mayo clinic-6 standard form.;Quality of life. Timepoint: in at the beginning of the study and after 2 months of treatment. Method of measurement: IBDQ-9(Farsi version).;CRP test. Timepoint: Before the intervention and end of the intervention(2 months). Method of measurement: Device.;Fecal calprotectin. Timepoint: Before the intervention and end of the intervention(2 months). Method of measurement: stool exam.
- Secondary Outcome Measures
Name Time Method Side effect. Timepoint: daily. Method of measurement: drug side effect registration questionnaire.