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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT02216994 |
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Date of registration:
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06/08/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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A New Scoring System Improves Diagnostic Accuracy of Intestinal Dysganglionosis --a Prospective Study
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Scientific title:
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Efficacy and Accuracy of a New Diagnostic Scoring System to Differentiate Hirschsprung Disease From Hirschsprung Disease Allied Disorders in the Patients With Suspected Intestinal Dysganglinosis: a Prospective Study |
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Date of first enrolment:
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January 2013 |
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Target sample size:
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80 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT02216994 |
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Study type:
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Interventional |
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Study design:
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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Phase:
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N/A
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Countries of recruitment
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China
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Contacts
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Name:
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Jiexiong Feng, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Tongji Medical College,Huazhong University of Science and Technology |
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Name:
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Hongyi Zhang, MD |
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Address:
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Telephone:
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27-83665209 |
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Email:
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zhanghongyidoc@gmail.com |
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Affiliation:
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Name:
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Hongyi Zhang, MD |
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Address:
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Telephone:
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27-83665209 |
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Email:
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zhanghongyidoc@foxmail.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Hard or firm stools for 2 or less per week
- Age are from newborn to 3 years old
Exclusion Criteria:
- Children>3 years of age
- Patients presented severe inflammation or malnutrition, unconsciousness or
perforation of intestine
Age minimum:
N/A
Age maximum:
3 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Hirschsprung Disease
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Intervention(s)
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Drug: high dose lactulose
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Drug: paraffin oil
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Behavioral: conservative treatment
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Primary Outcome(s)
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the predicting score calculation
[Time Frame: 6-12 months]
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Secondary Outcome(s)
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pathological diagnosis
[Time Frame: 12-18 months]
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Secondary ID(s)
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tj2014701
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TJCD-D-13-00074
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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