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Clinical Trials/NCT07212153
NCT07212153CompletedNot Applicable

The Effect of Preoperative Oral Carbohydrate Loading on Insulin Resistance in Adult Patients Undergoing Cardiac Surgery

Rifdhani Fakhrudin Nur1 site in 1 country50 target enrollmentStarted: January 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
50
Locations
1
Primary Endpoint
HOMA-IR (Homeostasis Model Assessment for Insulin Resistance)

Study Overview

Brief Summary

The goal of this clinical trial is to investigate the effect of preoperative oral carbohydrate on insulin resistance in adult cardiac surgery patients with a cardiopulmonary bypass machine. Insulin resistance is when the body does not respond well to insulin, which can raise blood sugar and slow recovery.

The main question this study aims to answer is:

Does drinking a carbohydrate drink 2 hours before surgery lower insulin resistance compared to drinking only water after on pump cardiac surgery?

Researchers will compare two groups:

One group will drink 400 milliliters of a maltodextrin (carbohydrate) drink (CL group). The other group will drink 400 milliliters of water (PL group).

Participants will:

  1. Be randomly assigned to one of the two groups.
  2. Have blood samples taken to measure insulin and glucose before and after surgery (at hour-0, and hour-24 after ICU admission).
  3. Be monitored in the intensive care unit for 24 hours after surgery.

Detailed Description

This prospective, randomized controlled trial is designed to evaluate whether preoperative oral carbohydrate loading reduces perioperative insulin resistance in adults undergoing elective cardiac surgery at Dr. Sardjito Hospital, Yogyakarta, Indonesia. Fifty participants aged 20-60 years with American Society of Anesthesiologists (ASA) physical status II-III will be randomly assigned to one of two groups:

  1. Intervention group (Carbohydrate Loading, CL): participants will receive 400 milliliters of a maltodextrin-based carbohydrate drink 2 hours before anesthesia.
  2. Control group (Placebo Loading, PL): participants will receive 400 milliliters of plain water 2 hours before anesthesia.

All participants will follow standard preoperative fasting guidelines. Blood samples for glucose and insulin will be taken immediately after induction of anesthesia, upon ICU admission (hour 0), and at hour 24 in the ICU. The main outcome is the Homeostatic Model Assessment of Insulin Resistance (HOMA-IR). Secondary outcomes include perioperative glucose levels and postoperative insulin requirements.

Randomization is computer-generated, with allocation concealed until assignment. Surgeons, anesthesiologists, ICU staff, outcome assessors, and data analysts will be blinded to group allocation. The sample size of 50 participants (25 per group) was calculated based on prior effect sizes, with 80% power and a two-sided alpha of 0.05.

Data will be analyzed using descriptive statistics and appropriate tests for continuous and categorical variables. Between-group comparisons will use Student's t-test or Mann-Whitney U test as appropriate. Normality will be assessed by Shapiro-Wilk test. Repeated measures will be analyzed with paired tests or ANCOVA models. A p-value <0.05 will be considered statistically significant.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Masking Description

This study is double-blind. Participants, care providers (surgeons, anesthesiologists, ICU staff), investigators, outcome assessors, data collectors, and analysts were blinded to group allocation. Only the designated study staff who handled randomization and intervention preparation had access to allocation information.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age 20 to 60 years
  • •ASA physical status II or III
  • •Good tolerance to enteral fluid administration

Exclusion Criteria

  • •History of diabetes mellitus
  • •Thyroid insufficiency
  • •Adrenal insufficiency
  • •Gastroesophageal reflux disease
  • •Emergency cardiac surgery
  • •Dropout criteria:
  • •Participant withdraws consent
  • •Cardiac surgery duration exceeds 4 hours

Arms & Interventions

Carbohydrate Loading (CL)

Experimental

Participants receive 400 mL of a maltodextrin-based carbohydrate drink 2 hours before surgery. The drink contains 50 g of carbohydrate (maltodextrin).

Intervention: Oral Carbohydrate Drink (Maltodextrin) (Dietary Supplement)

Placebo Loading (PL)

Placebo Comparator

Participants receive 400 mL of plain water 2 hours before surgery, following the same timing and fasting protocol as the experimental group.

Intervention: Placebo (Water) (Other)

Outcomes

Primary Outcomes

HOMA-IR (Homeostasis Model Assessment for Insulin Resistance)

Time Frame: baseline, 0 hour ICU admission, and 24 hours ICU admission

The Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) is calculated as fasting insulin (µU/mL) × fasting glucose (mmol/L) / 22.5. Higher values indicate greater insulin resistance.

Secondary Outcomes

  • Perioperative Blood Glucose Levels(baseline, 0 hour ICU admission, and 24 hours ICU admission)
  • Perioperative Serum Insulin Concentration(baseline, 0 hour ICU admission, and 24 hours ICU admission)

Investigators

Sponsor
Rifdhani Fakhrudin Nur
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Rifdhani Fakhrudin Nur

Principal Investigator

Gadjah Mada University

Study Sites (1)

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