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Colonoscopy preparation and probiotic use on the severity of constipatio

Phase 2
Conditions
Functional constipation.
Constipation
K59.0
Registration Number
IRCT20210817052219N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
74
Inclusion Criteria

Having functional constipation in people over 18 years according to ROME IV criteria
Having irritable bowel syndrome with constipation patternaccording to ROME IV criteria
Free and informed written consent to participate in the study
Age over 18 years

Exclusion Criteria

Any history of chronic inflammatory disease or structural disease of the gastrointestinal tract
Any serious physical problems or illnesses such as inflammation or malignancy
Any physical problems that prevent you from doing physical activity
Addiction to drugs or sleeping pills
History of chronic diseases such as diabetes

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Constipation score. Timepoint: Before receiving the colonoscopy preparation and then in weeks 2, 4, 8 after the start of the intervention and 4 weeks after the end of the intervention (week 12). Method of measurement: ROM 3 criteria.
Secondary Outcome Measures
NameTimeMethod
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