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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05785013
Other study ID # MS 277-2022
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2023
Est. completion date July 2, 2023

Study information

Verified date February 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

1. Pre operative anthropometric assessment including : weight in kg, height/length and BMI 2. Pre operative Zinc supplementation (dose according to the age) for 7 days preoperatively for cases 3. Postoperative data collection


Description:

Postoperative data collection : - Length of hospital stay - Complication and sorting of them - Lab withdrawal of inflammatory markers on 2-3 day postoperatively


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date July 2, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 1 Month to 12 Years
Eligibility Inclusion Criteria: 1. All children patients with Hirschsprung disease admitted for surgical intervention with different ( age , sex ) 2. Type of surgery : transanal pull through 3. Whose parents or caregivers approve for the participation in the study Exclusion Criteria: 1. Patients with emergency situations 2. Whose parents or caregivers will not apply for the participation in the study

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Zinc
Zinc Supplementation

Locations

Country Name City State
Egypt Hoda Atef Abdelsattar Ibrahim Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The effect of preoerative Zinc supplementation on the hospital length stay in children operated for Hirschsprung's disease Children oprated for elective surgery for Hirschsprung's disease will be supplemented with zinc seven days before surgery and postoperative data as the duration of hospital length stay in hours will be meausred in both the cases and control groups and comapred. zinc supplemenation for one week
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