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Trials / Completed

CompletedNCT05785013

The Impact of Preoperative Supplementation of Zinc

The Impact of Preoperative Supplementation of Zinc on Post-operative Outcomes in Children Undergoing Elective Surgery for Hirsch Sprung Disease

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
1 Month – 12 Years
Healthy volunteers
Not accepted

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

Detailed description

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

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTZincZinc Supplementation

Timeline

Start date
2023-04-01
Primary completion
2023-06-30
Completion
2023-07-02
First posted
2023-03-27
Last updated
2024-02-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05785013. Inclusion in this directory is not an endorsement.

The Impact of Preoperative Supplementation of Zinc (NCT05785013) · Clinical Trials Directory