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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02255747
Other study ID # Anal Dilatation
Secondary ID
Status Recruiting
Phase N/A
First received September 28, 2014
Last updated September 30, 2014
Start date September 2014
Est. completion date October 2016

Study information

Verified date September 2014
Source Tongji Hospital
Contact Zhi Li, MD PhD
Phone +8613387664883
Email lizhimdphd@163.com
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This study is to evaluate the effect of anal dilation in infants and children with constipation.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date October 2016
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender Both
Age group 1 Month to 14 Years
Eligibility Inclusion Criteria:

1. Infants and Children With Constipation

2. Postoperative infants and children with Hirschsprung's disease

3. Good compliance

Exclusion Criteria:

1. Infants and Children With Constipation

2. Poor compliance

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Lactulose


Locations

Country Name City State
China Tongji Hospital Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Tongji Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Daily stool times two years No
Secondary The frequency of intestinal peristalsis waves two years No
Secondary The amplitude of intestinal peristalsis waves two years No
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