Impact on outcome of glycemic control in diabetic patients undergoing open heart surgery

Comparison of patients? outcome in open cardiac surgery with two methods of blood glucose control:1-Thigt 2-Conventional

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013041713052N1

Enrollment

Registered

2013-07-09

Start date

2013-03-19

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

daiabetes. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: In the intervention group, glycemic control using insulin to target blood glucose100- 120 done. Intervention 2: In the control group, the treatment of blood glucose greater than 200 ta

Treatment - Drugs

In the intervention group, glycemic control using insulin to target blood glucose100- 120 done

In the control group, the treatment of blood glucose greater than 200 target value 180-200mg/dl.

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Diabetes; Age:18-70; ASA 2-3; All of on pomp cardiac surgery Exclusion criteria: Off pomp cardiac surgery; Ketoasidosis or Hyperosmolar coma; Redosurgery; History of TIA or CVA

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Dedth. Timepoint: in the ICU and after 30 days. Method of measurement: Observation of ECGflat.;Wound infection. Timepoint: in the ICU and after 30 days. Method of measurement: Observation.;Mecanical ventilation time. Timepoint: in the ICU. Method of measurement: hours after arival in the ICU.;Cardiac aritmia. Timepoint: in the ICU and after 30 days. Method of measurement: with ECG.;Strock. Timepoint: in the ICU and after 30 days. Method of measurement: with symptoms.;ARF. Timepoint: in the ICU and after 30 days. Method of measurement: WITH BUN,cr.	—

Measure

Time frame

Dedth. Timepoint: in the ICU and after 30 days. Method of measurement: Observation of ECGflat.;Wound infection. Timepoint: in the ICU and after 30 days. Method of measurement: Observation.;Mecanical ventilation time. Timepoint: in the ICU. Method of measurement: hours after arival in the ICU.;Cardiac aritmia. Timepoint: in the ICU and after 30 days. Method of measurement: with ECG.;Strock. Timepoint: in the ICU and after 30 days. Method of measurement: with symptoms.;ARF. Timepoint: in the ICU and after 30 days. Method of measurement: WITH BUN,cr.

—

Secondary

Measure	Time frame
ICU staying. Timepoint: from arival to discharg from ICU. Method of measurement: DAY.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Fatemeh Javaherforoosh Zadeh

Joundishapoor University Of Medical Sciences

javaherforoosh-f@ajums.ac.ir+61 13919315

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 19, 2026