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To study the effect of the drug Dexmedetomidine on fluctuations in Blood glucose levels in Diabetic Patients who are undergoing Off Pump Coronary Artery Bypass Grafting

Effect Of Dexmedetomidine On Glucose Variability In Diabetic Patients Following Off Pump Coronary Artery Bypass Grafting - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/068085
Enrollment
68
Registered
2024-05-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Inj. Dexmedetomidine at 0.5 mcg/kg/hour: Inj. Dexmedetomidine at 0.5 mcg/kg/hour in Group D(DEXMEDETOMIDINE) given after induction till end of surgery Control Intervention1: Inj. 0.9% N

Sponsors

Iti Shri
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: diabetic patients with HbA1c less than or equal to 8% with fasting blood sugar of less than 150mg/dl ejection fraction of more than 50% undergoing elective off pump coronary artery bypass grafting(CABG)

Exclusion criteria

Exclusion criteria: diabetic patients with HbA1c more than 8% with fasting blood sugar of more than 150mg/dl,emergency CABG,CABG done on cardiopulmonary bypass or if intraoperative pump conversion, CABG done with other heart surgeries, anemia with preoperative Hb less than 10g%, Hepatic dysfunction, patients on preoperative steroids, an endocrine disorder with hypercortisolism, bradycardia due to any reason, any active infection, patient critically ill like on mechanical ventiation or inotropes or intra aortic balloon pump

Design outcomes

Primary

MeasureTime frame
To assess the effect of injection dexmedetomidine on blood glucose variabilityTimepoint: After induction till 24 hours

Secondary

MeasureTime frame
1.To assess the level of inflammatory markers viz.IL-6 and CRP at preinduction, and at 12 hours and 24 hours postoperatively. 2.To assess and compare mean insulin requirement between the groups.Timepoint: 24 hours postoperatively

Countries

India

Contacts

Public ContactIti Shri

ABVIMS and Dr. RML Hospital, New Delhi

itianesthesia@gmail.com9212400570

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026