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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
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05785013
Enrollment
1
Registered
2023-03-27
Start date
2023-04-01
Completion date
2023-07-02
Last updated
2024-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutrition Disorders, Surgery

Brief 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

Interventions

DIETARY_SUPPLEMENTZinc

Zinc Supplementation

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
1 Months to 12 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
The effect of preoerative Zinc supplementation on the hospital length stay in children operated for Hirschsprung's diseasezinc supplemenation for one weekChildren 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.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026