Glucose Insulin Potassium With Intensive Insulin Therapy and (GIK2) Versus GIK Alone

Sponsor
University of Monastir (Other)
Overall Status
Completed
CT.gov ID
NCT00965406
Collaborator
(none)
772
3
3
46
257.3
5.6

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the effect of the glucose insulin potassium (GIK) infusion associated with intensive insulin therapy compared to GIK alone and control group in patients presenting to the ED with acute coronary syndrome.

Condition or Disease Intervention/Treatment Phase
  • Drug: GIK and intensive insulin therapy
Phase 3

Detailed Description

It is well recognised that diabetes is a factor of worse prognosis in acute coronary syndrome (ACS). Recently, the relationship between the glucidic metabolism and cardiac ischemia was highlighted whether patients have diabetes or not. Indeed, it was established that hyperglycemia occurring during hospitalization in non diabetic patients, is a powerful risk factor of death.

Stress related hyperglycemia occurs during number of acute pathological situations (AMI, stroke, pancreatitis, hypothermia, hypoxia, cirrhosis, polytrauma, burn, sepsis…. It is due to an excess of hyperglycemia hormones (glucagon, growth hormone, catecholamines and glucosteroids) and of inflammatory mediators (cytokines…). Hyperglycemia has several deleterious effects on the cardiovascular system as it promotes microvascular inflammatory reaction, activation of the coagulation system, and free radical oxygen liberation.

Currently, the idea of controlling glycemia in surgical and medical intensive care patients is widely accepted and maintaining blood sugar level closest to normal by intensive insulin therapy became largely recommended.

Several decades ago, glucose-insulin-potassium infusion (GIK) was proposed to protect acute cardiac ischemia. GIK has been assessed in many previous studies.

The results of these studies are contradictory. According to CREATE-ECLA study which is the largest (including 20201 patients), GIK didn't show a significant beneficial effect in ACS. However, in these trials using GIK alone glycemia was not strictly controlled.

Recently, the importance of tight glycemic control has been highlighted in ICU patients and early post heart surgery. Our hypothesis is that GIK treatment associated to intensive insulin therapy in ACS would be beneficial and superior to GIK alone possibly because intensive insulin therapy would prevent potential deleterious effects of hyperglycemia induced by GIK.

Study Design

Study Type:
Interventional
Actual Enrollment :
772 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Glucose Insulin Potassium With Intensive Insulin Therapy and (GIK2) Versus GIK Alone in the Early Management of Acute Coronary Syndrome: Randomised Controlled Study
Study Start Date :
Aug 1, 2010
Actual Primary Completion Date :
Dec 1, 2013
Actual Study Completion Date :
Jun 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: glucose insulin potassium (GIK)

Glucose + insulin +6 potassium (GIK) infusion (1000 ml of Glucose 10%, 20 UI Insulin, 70 mEq of Potassium) within 24 hours.

Drug: GIK and intensive insulin therapy
GIK infusion (1000 ml of Glucose 10%, 20 UI Insulin, 70 mEq of Potassium) within 24 hours. Intravenous intensive insulin therapy is simultaneously administered according to our protocol in the ED
Other Names:
  • GIKI2
  • Experimental: GIK and intensive insulin therapy

    GIK infusion (1000 ml of Glucose 10%, 20 UI Insulin, 70 mEq of Potassium) within 24 hours. Intravenous intensive insulin therapy is simultaneously administered according to our protocol in the ED

    Drug: GIK and intensive insulin therapy
    GIK infusion (1000 ml of Glucose 10%, 20 UI Insulin, 70 mEq of Potassium) within 24 hours. Intravenous intensive insulin therapy is simultaneously administered according to our protocol in the ED
    Other Names:
  • GIKI2
  • No Intervention: Control group

    No intervention and patients were treated with updated international recommendations of acute coronary syndrome.

    Outcome Measures

    Primary Outcome Measures

    1. 30 days mortality, reinfarction, urgent coronary revascularisation, and stroke. [24 hours]

    Secondary Outcome Measures

    1. Severe dysrhythmias, acute left ventricular failure with ejection fraction<45%, serum troponin, PAI level and platelet factor activator (PFA-100) within 24 hours after the start of protocol treatment. Safety: major or minor hypoglycemia [24 hours]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All patients fulfilling ACS criteria with or without known diabetes.
    Exclusion Criteria:
    • Patients under 18 years old.

    • Killip II class or SaO2 ≤ 90%.

    • Blood creatinine ≥ 180 µmol/L

    • Potassium serum ≥ 6.5 mmol/L.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mahdia University Hospital Monastir Mahdia Tunisia
    2 Monastir University Hospital Monastir Tunisia 5000
    3 Sahloul University Hospital Sousse Tunisia

    Sponsors and Collaborators

    • University of Monastir

    Investigators

    • Principal Investigator: nouira semir, Prof., Research Laboratory (LR12SP18) University of Monastir Tunisia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Pr. Semir Nouira, Prof. Semir Nouira, University of Monastir
    ClinicalTrials.gov Identifier:
    NCT00965406
    Other Study ID Numbers:
    • GIKI2
    First Posted:
    Aug 25, 2009
    Last Update Posted:
    May 2, 2017
    Last Verified:
    Apr 1, 2017
    Keywords provided by Pr. Semir Nouira, Prof. Semir Nouira, University of Monastir
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 2, 2017