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Impact of Vitamin C Supplementation on Hospital Outcomes in Children Undergoing Corrective Heart Surgery for Congenital Heart Diseases (RCT)

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

Congenital Heart Disease (CHD)

Treatments

Other: Vitamin C
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT06789640
MS-588-2023 (Other Identifier)

Details and patient eligibility

About

Vitamin C will be given before admission in the immediate preoperative preceding 7 days (the dose 30 -45 mg per day ) in oral drops preparations

Inflammatory markers including CRP , TLC ,PNI , GPS NLR will be checked on admission and on discharge and compared between cases and controls Hospital length stay will also be compared between the two groups

Enrollment

20 estimated patients

Sex

All

Ages

Under 7 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children in the first two years who will be for corrective surgery for heart diseases congenital heart diseases
  • Pediatric patients whose parents or caregivers agree to be enrolled in the study.
  • Risk Adjustment for Congenital Heart Surgery -1 (RACHS-1) for Evaluation of Mortality in Children Undergoing Cardiac Surgery : the first two categories (Thiagarajan and C. Laussen 2015)

Exclusion criteria

  • Pediatric patients with associated comorbid conditions.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 2 patient groups, including a placebo group

Interventional
Experimental group
Description:
Vitamin C will be given before admission in the immediate preoperative preceding 7 days (the dose 30 -45 mg per day ) in oral drops preparations Inflammatory markers including CRP , TLC ,PNI , GPS NLR will be checked on admission and on discharge and compared between cases and controls Hospital length stay will also be compared between the two groups
Treatment:
Other: Vitamin C
The control group
Placebo Comparator group
Description:
A placebo will be given before admission in the immediate preoperative preceding 7 days (the dose 30 -45 mg per day ) in oral drops preparations Inflammatory markers including CRP , TLC ,PNI , GPS NLR will be checked on admission and on discharge and compared between cases and controls Hospital length stay will also be compared between the two groups
Treatment:
Other: Placebo

Trial contacts and locations

0

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Central trial contact

Hoda Atef Abdelsattar Ibrahim

Data sourced from clinicaltrials.gov

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