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The Effect of Preoperative Oral Carbohydrate Administration on Perioperative Hypothermia in Pediatric Patients

B

Başakşehir Çam & Sakura City Hospital

Status

Completed

Conditions

Perioperative Hypothermia

Study type

Observational

Funder types

Other

Identifiers

NCT06428604
2019/64

Details and patient eligibility

About

Hypothermia that may develop in the perioperative period is associated with many adverse clinical outcomes. In particular, pediatric patients were more susceptible to hypothermia and related complications such as respiratory distress, metabolic acidosis, hypoglycemia, hypoxemia, cardiac disorders, coagulopathy, and wound infection than adults. In this study, the effect of preoperative carbohydrate-rich feeding on temperature regulation in pediatric patients was investigated.

Enrollment

2 patients

Sex

All

Ages

2 to 15 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients to be operated on by the Department of Pediatric Surgery
  2. Being between the ages of 2 and 15
  3. Not restricting oral intake
  4. ASA I-II-III patients in anesthesia risk score
  5. Patients operated between 01.03.2019 and 31.07.2019
  6. Not having any communication problems (mental retardation, not knowing Turkish, etc.)
  7. Not having gastroesophageal reflux
  8. Not having any muscle disease
  9. Informed volunteer consent must be obtained
  10. Patients for whom emergency surgery is not planned
  11. No disease related to the central nervous system

Exclusion criteria

  1. Pediatric patients outside the 2-15 age range
  2. Having limited oral intake
  3. ASA IV and above in anesthesia risk scoring
  4. Patients operated before 01.03.2019 or after 31.07.2019
  5. Patients who may have communication problems with their parents or themselves
  6. Patients with gastroesophageal reflux
  7. Patients with muscle disease
  8. Patients for whom informed voluntary consent has not been obtained
  9. Patients who will undergo emergency surgery
  10. Patients with diseases related to the central nervous system

Trial design

2 participants in 2 patient groups

GRUP W
Description:
patient group given only 5 ml kg-1 oral water 3 hours before the surgery,
GRUP C
Description:
Patient group given 5 ml kg-1 clear carbohydrate-rich liquid orally 3 hours before surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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