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The effect of polyethylene glycol and lactulose in children with constipatio

Phase 3
Recruiting
Conditions
Constipation.
Constipation, unspecified
K59.00
Registration Number
IRCT20190717044239N1
Lead Sponsor
Vice Chancellor of Research and Technology Shahrekord University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
94
Inclusion Criteria

Chronic functional constipation

Exclusion Criteria

Ileus
Renal failure
Heart failure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Constipation. Timepoint: Before the intervention and after 7, 14 and 21 days. Method of measurement: Checklist.
Secondary Outcome Measures
NameTimeMethod
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