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The effect of rhythmic breathing on hyperglycemic control after coronary artery bypass graft surgery in non-diabetic patients

The effect of rhythmic breathing on hyperglycemic control after coronary artery bypass graft surgery in non-diabetic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120109008665N7
Enrollment
60
Registered
2018-09-03
Start date
2018-09-06
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

Hyperglycemia. Hyperglycemia, unspecified

Interventions

Intervention 1: Intervention group: For patients in this group before surgery, this respiratory technique is trained individually to a degree to mastery that has the ability to perform independently a

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1- Glycosylated hemoglobin less than 7% 2- Blood glucose greater than 150 mg / dl 3- Elective coronary artery bypass surgery 4- Age between 35 and 75 years 5- Stable hemodynamic status (BP> 90 mmHg and PR between 50 and 110) 6- Use Cardiopulmonary Bypass

Exclusion criteria

Exclusion criteria: 1- History of diabetes 2- Life threatening arrhythmias 3-Long-term intubation (more than 24 hours after surgery) 4- Dependence on inotropic agents for hemodynamic stability after extubation 5. The level of potassium is higher than 5/5 or lower than 5/3 when admitted in the ICU 6- Pao2 Less than 60 mm Hg without oxygen supply through nasal cannula or mask 7. Renal function disorders before and after surgery

Design outcomes

Primary

MeasureTime frame
Decrease blood glucose. Timepoint: Blood glucose levels will be measured at 6 am (fasting blood sugar), 10 am, 4 pm and 10 am through the laboratory and after providing 2 cc of the patient's blood. Method of measurement: Send patient blood samples to the laboratory.

Secondary

MeasureTime frame
Pain severity in sternotomy site. Timepoint: Pain severity will be measured at 9 a.m. and 9 p.m. on three consecutive days. Method of measurement: Using visual analog scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHassan Babamohamadi

Semnan University of Medical Sciences

babamohamadi@semums.ac.ir+98 23 3365 4192

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 15, 2026