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Postoperative NT –proBNP level in coronary artery bypass surgery with ventricular dysfunction after perioperative GIK treatment

Postoperative NT –proBNP level in coronary artery bypass surgery with ventricular dysfunction after perioperative GIK treatment

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201008223438N1
Enrollment
60
Registered
2010-10-05
Start date
2010-09-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: patients with low ejection fraction, undergoing isolated on pump coronary artery bypass surgery (CABG). Condition 2: Ischaemic heart diseases. - Ischaemic heart diseases

Interventions

Intervention 1: The GIK group received GIK solution (500 ml DW10% + 40U regular insulin+40 mEq KCl and 2gr MgSO4) at a rate of 50 ml/h for 10 hours preoperatively until the removal of aortic cross cla
Treatment - Drugs
The GIK group received GIK solution (500 ml DW10% + 40U regular insulin+40 mEq KCl and 2gr MgSO4) at a rate of 50 ml/h for 10 hours preoperatively until the removal of aortic cross clamp
The control group received half saline solution as placebo with an equivalent infusion rate during the same duration.

Sponsors

Research Deputy, School of Medicine, Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: elective first-time CABG with cardiopulmonary bypass (CPB), LVEF=40%; as assessed by preoperative echocardiography) and patient consent for entering the study exclusion criteria: diabetics, patients who required concomitant valvular heart surgery, preoperative use of cardiovascular support (inotropes and/or an intraaortic balloon pump), or a serum creatinine level of >200 µmol/L were considered as exclusion criteria

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Measurement of serum NT-proBNP levels. Timepoint: before the initiation of the solutions, at the time of anesthesia induction and 24h after surgery. Method of measurement: Roche Elecsys assay.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnoosh Foroughi

Research and Developement Center

m_foroughi@sbmu.ac.ir+98 21 2236 0635

Outcome results

None listed

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