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The effect of preoperative incentive spirometry (IS) on postoperative pain intensity, respiratory parameters, and quality of recovery in patients undergoing Coronary Artery Bypass Graft

The effect of preoperative incentive spirometry (IS) on postoperative pain intensity, respiratory parameters, and quality of recovery in patients undergoing Coronary Artery Bypass Graft

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240706062346N1
Enrollment
100
Registered
2024-07-23
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Coronary artery bypass graft. Atherosclerosis of coronary artery bypass graft(s) and coronary artery of transplanted heart with angina pectoris

Interventions

Intervention 1: Intervention group: In this group, incentive spirometry will be used for 2 days before surgery, and after surgery, there will be no difference with the control group. Incentive spirome
Take a few normal breaths. hold the incentive spirometer in his hands vertically facing his face
Put the mouthpiece in your mouth and tighten your lips around it
Now breathe as slowly and deeply as possible and look at the yellow piece inside the chamber that rises. A smaller piece in the spirometer looks like a ball or disc. Your goal should be to keep the ba

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Having informed consent to participate in the study Age group 18 to 70 years Having stable vital signs and hemodynamics when completing the questionnaires Sufficient consciousness to answer the question The patient's CABG surgery should be Off-Pump type.

Exclusion criteria

Exclusion criteria: Conditions for emergency CABG surgery for any reason, including coronary dissection during angiography Existence of simultaneous conditions for combined surgeries such as CABG and valve replacement and repair at the same time Cardiac disorders and congenital anomalies Severe respiratory disorders that affect oxygenation and ventilation, such as severe COPD Having a clear mental disorder and severe mood-emotional disorder that prevents effective communication. Patients who have previously had surgery in the thorax area, such as previous CABG, lobectomy, etc.

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: At the beginning of the study and 12, 24, 48 and 72 hours after the end of surgery. Method of measurement: Visual analog scale.;Respiratory parameters. Timepoint: At the beginning of the study and 12, 24, 48 and 72 hours after the end of surgery. Method of measurement: Arterial sampling for ABG and its respiratory parameters as well as patient bed monitoring.;Quality of recovery. Timepoint: At the beginning of the study and 72 hours after the end of surgery. Method of measurement: Quality of Recovery - 15.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Saboorifar

Sabzevar University of Medical Sciences

saboorifarh01@medsab.ac.ir+98 51 4401 1000

Outcome results

None listed

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