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Preoperative Two Hours Carbohydrate Load On Pediatric Patient Undergoing Elective Surgery

Effect of Preoperative Two Hours Carbohydrate Load On Pediatric Patient Undergoing Elective Surgery: A Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06833671
Enrollment
90
Registered
2025-02-19
Start date
2022-06-01
Completion date
2024-10-21
Last updated
2025-02-19

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

Conditions

Preoperative, Carbohydrate, Pediatric, Elective Surgery

Brief summary

This work evaluated the systemic effect of different preoperative carbohydrate (CHO) loads in pediatrics undergoing elective surgery.

Detailed description

Children undergoing surgery experience stress due to disruptions in their daily routine and exposure to various perioperative circumstances that induce anxiety and pain. The management of perioperative nutrition in pediatric patients is a crucial aspect of patient care. The concept of preoperative carbohydrate (CHO) loading has gained attention as a potential strategy to mitigate these drawbacks. The administration of a CHO-rich drink two hours preoperative has been proposed to maintain euglycemia, decline IR, and enhance postoperative recovery

Interventions

A preoperative carbohydrate load was done two hours before the operation using a10 ml/kg, with a maximal volume of 250 ml of commercial brand of apple juice (glucose 28 g in 250 ml).

A preoperative carbohydrate load was done using 1.75mg/kg/dose of anhydrous glucose (Alpha Chmika).

OTHERWater

Patients received water.

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
5 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

* Age from 5 to 10 years. * Both sexes. * American Society of Anesthesiologists (ASA) physical status I and II. * Scheduled for elective surgery.

Exclusion criteria

* Diabetes mellitus. * Insulin resistance (IR). * Renal or hepatic insufficiency. * Esophageal or gastric surgery or gastrointestinal disorders history (including gastroesophageal reflux, hiatal hernia, or gastritis).

Design outcomes

Primary

MeasureTime frameDescription
C-reactive protein (CRP) level4 hours postoperativelyC-reactive protein (CRP) level was assessed two h before surgery as baseline, at induction of anesthesia, and 4 hours after the operation.

Secondary

MeasureTime frameDescription
Level of procalcitonin4 hours postoperativelyLevel of procalcitonin was assessed two h before surgery as baseline, at induction of anesthesia, and 4 hours after the operation.
Homeostatic model assessment for insulin resistance4 hours postoperativelyHomeostatic model assessment for insulin resistance(HOMA.IR) was assessed two h before surgery as baseline, at induction of anesthesia, and 4 hours after the operation.
Level of C-peptide4 hours postoperativelyLevel of C-peptide was assessed two h before surgery as baseline, at induction of anesthesia, and 4 hours after the operation.
Neutrophil/ lymphocyte ratio4 hours postoperativelyNeutrophil/ lymphocyte ratio (NLR) was assessed 2 h before surgery as baseline, at induction of anesthesia, and 4 hours after the operation.
Patient's parent's satisfaction4 hours postoperativelyParent satisfaction level was evaluated by 3-point Likert scale (1, unsatisfied; 2, neutral; 3, satisfied).
Incidence of complications4 hours postoperativelyIncidence of complications such as perioperative nausea, vomiting, and aspiration were documented.
Level of random blood glucoseTwo hours before the surgeryLevel of random blood glucose (RBG) was measured at two hours before the surgery.

Countries

Egypt

Outcome results

None listed

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