Effect of viseral manipulation in constipatio

Not Applicable

• Conditions: Constipation.; Functional intestinal disorder, unspecified; K59.9

• Registration Number: IRCT20190614043891N1
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 December 2019

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

All children with Functional constipation aged 5 to 18 years
At least 3 months have passed since they occurred

Exclusion Criteria

Endocrine and Metabolic disorders (eg, Hypothyroidism, Hypercalcemia, Diabetes mellitus)
Neurologic and Psychiatric disorders(Spina bifida, Cerebral palsy, Autism)
Hirschsprung’sdisease and Down’s syndrome
Congenital anorectal malformation

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Bristol scale score that measure the consistency and shape of the stool. Timepoint: At the beginning of the study (before the intervention) and 28 days after the intervention. Method of measurement: Bristol Stool Form Scale.;Score of defecation pain. Timepoint: At the beginning of the study (before the intervention) and 28 days after the intervention. Method of measurement: Wong-Baker Faces Pain Rating Scale.;Score of abdominal pain. Timepoint: At the beginning of the study (before the intervention) and 28 days after the intervention. Method of measurement: Wong-Baker Faces Pain Rating Scale.;Number of defecation per week. Timepoint: At the beginning of the study (before the intervention) and 28 days after the intervention. Method of measurement: Patient report.

Secondary Outcome Measures

Name	Time	Method
Dosage of laxative drug. Timepoint: At the beginning of the study (before the intervention) and 28 days after the intervention. Method of measurement: Patient report.