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Efficacy of Carbohydrate Loading in Diabetic Type 2 Patients Undergoing CABG Surgery on CPB

Efficacy of Carbohydrate Loading in Diabetic Type 2 Patients Undergoing CABG Surgery on CPB

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06951308
Acronym
CLDM-CABG
Enrollment
50
Registered
2025-04-30
Start date
2025-04-01
Completion date
2026-12-31
Last updated
2026-09-01

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

Conditions

Heart Surgery, Ischemic Heart Disease

Keywords

Enhanced recovery program, carbohydrate loading, coronary artery bypass grafting, heart surgery, postoperative recovery

Brief summary

Enhanced recovery after surgery protocols aim to optimize perioperative care and improve surgical outcomes. Preoperative carbohydrate loading has demonstrated benefits in reducing insulin resistance and improving patient outcomes. While non-diabetic patients benefit from this approach, its efficacy in diabetic type 2 patients undergoing CABG remains less understood. This study aims to address this gab by evaluating the physiological and clinical outcomes for carbohydrate loading in this specific population.

Detailed description

A randomized controlled trial comparing diabetic type 2 patients receiving carbohydrate loading with those undergoing traditional fasting protocols. Patients will be randomized to two groups; group (a) patients will have carbohydrate loading 2 hours before the surgery (400 ml of 12.5 maltodextrin and 400 ml of over-the-counter fruit-based lemonade), while group (b) patients (control group) will have standard fasting protocol 8 hours before surgery. Aims of the study: 1. To assess the efficacy of carbohydrate loading in reducing insulin resistance in diabetic type 2 patients undergoing CABG surgeries. 2. To monitor clinical outcomes such as infection rates, ICU stay duration, and need for inotropic and vasoactive drugs. 3. To evaluate changes in inflammatory markers including CRP levels. clinical outcome

Interventions

DIETARY_SUPPLEMENTCarbohydrate loading before surgery

Carbohydrate loading 2 hours before the surgery (400 ml of 12.5 maltodextrin and 400 ml of over-the-counter fruit-based lemonade)

Sponsors

Damascus University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

All diabetic type 2 patients undergoing isolated on-pump coronary artery bypass surgery.

Exclusion criteria

* Missing data. * Patients outside the study period. * Patients undergoing other cardiac surgeries. * Patients diagnosed with type 1 diabetes mellitus.

Design outcomes

Primary

MeasureTime frameDescription
Short Insulin Tolerance Test (KITT)Preoperatively and up to 72 hours postoperativelyShort Insulin Tolerance Test (KITT) will test changes in insulin tolerance postoperatively

Secondary

MeasureTime frameDescription
CRP levelsPreoperatively and up to 72 hours postoperativelyC-Reactive Protein levels in the blood
Arterial blood gasesPreoperatively and up to 72 hours postoperativelyChanges in arterial blood gases
Operative timeIntraoperatively, skin-to-skinTotal operative time, skin-to-skin
CPB durationIntraoperatively, using extracorporeal circulationTotal time spend using cardiopulmonary bypass perfusion
Blood lossIntraoperatively and up to 72 hours postoperativelyBlood loss and blood product usage
Number of grafts performedIntraoperatively, skin-to-skinNumber of grafts performed during the operation
Use of inotropsIntraoperatively and up to 72 hours postoperativelyUse of inotrops to support the cardiac output
ComplicationsIntraoperatively and up to 72 hours postoperativelyAll perioperative complications

Countries

Syria

Contacts

CONTACTMohammad B Izzat, FRCS(CTh)
mbizzat@gmail.com+963943240820
CONTACTMohammad S Sioufi, MD
m.s.sioufi@gmail.com+963967788163
STUDY_DIRECTORMohammad B Izzat, FRCS(CTh)

Damascus University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 2, 2026