Evaluation of the concurrent polyethylene glycol and probiotic in treatment of constipatio

Phase 2

• Conditions: Constipation.; Constipation; K59.0

• Registration Number: IRCT20171030037093N12
• Lead Sponsor: Vice chancellor for research, Shahrekord University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 August 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

Suffering from chronic functional constipation
Age from 2 to 15 years
Not being infected with large and small intestinal diseases
Insomnia to polyethylene glycol
Lack of bowel obstruction
The absence of kidney or heart failure

Exclusion Criteria

Creating diarrhea following a drug
Create unwanted allergic reactions after taking medication

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
nwanted exclusion. Timepoint: Before and during the first and second weeks after treatment. Method of measurement: Check list.;Excretion of stool. Timepoint: Before and during the first and second weeks after treatment. Method of measurement: Check list.;Painful exclusion. Timepoint: Before and during the first and second weeks after treatment. Method of measurement: Check list.;Stomach ache. Timepoint: Before and during the first and second weeks after treatment. Method of measurement: Check list.;Consistency. Timepoint: Before and during the first and second weeks after treatment. Method of measurement: Check list.