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Comparison of incentive spirometry and peak expiratory flow meter to evaluate cardiorespiratory parameters after valvular surgery

Comparison of incentive spirometry and peak expiratory flow meter to evaluate cardiorespiratory parameters after valvular surgery

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230123057185N1
Enrollment
64
Registered
2023-03-17
Start date
2023-03-24
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Heart valvular surgery. Aortic regurgitation, Aortic stenosis, Mitral stenosis, Mitral regurgitation, Marfan's syndrome, Rheumatic fever, Endocarditis, Atresia, Heart valve disease, Valvular heart disease, Valvular surgery

Interventions

Intervention 1: Intervention group 1: Incentive spirometry 1.The patient will be asked to lie flat on

Sponsors

Ch. Pervaiz Elahi Institute of Cardiology Hospital, Multan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients of both sexes i-e male and female Patients with age ranges of (35-65yrs.) Patients who have recently undergone extubated heart valve surgery and who will be able to comply with the instructions and sign the consent form. Patients who underwent median sternotomy-based valvular surgery. Patients with stable hemodynamics

Exclusion criteria

Exclusion criteria: Patients who needed to be intubated for more than 48 hours following surgery. Re-intubation throughout the healing process Patients who within the previous three months had a history of a respiratory infection Patients undergo CABG surgery. Patients with any neuromuscular disease, renal disease, smokers, alcohol, anemia, and pregnant females.

Design outcomes

Primary

MeasureTime frame
Blood Pressure. Timepoint: Before interventions and after 3 weeks of interventions. Method of measurement: Cardiorespiratory parameters like blood pressure will be measured by Arterial line.;Heart rate. Timepoint: Before interventions and after 3 weeks of interventions. Method of measurement: Cardiorespiratory parameters like heart rate will be measured by arterial line.;Respiratory rate. Timepoint: Before interventions and after 3 weeks of interventions. Method of measurement: Cardiorespiratory parameters like respiratory rate will be measured by arterial line.;ABG's ( Atrial blood gasses). Timepoint: Before interventions and after 3 weeks of interventions. Method of measurement: Cardiorespiratory parameters like ABG's (atrial blood gasses) will be measured by arterial line.;Oxygen saturation. Timepoint: Before interventions and after 3 weeks of interventions. Method of measurement: Oxygen saturation will be measured by probe of pulse oximeter.

Secondary

MeasureTime frame
Rating of perceived exertion. Timepoint: Before intervention and 3 weeks after intervention. Method of measurement: Rate of perceived exertion will be measured by Borg scale.;SF8 quality of life (A questionnaire). Timepoint: Before intervention and 3 weeks after intervention. Method of measurement: patients will fill the SF8 quality of life questionnaire.

Countries

Pakistan

Contacts

Public ContactDr. Farah Zahid

Muhammad Institute of medical and Allied sciences Multan

farahzahid977@gmail.com+92 306 1708076

Outcome results

None listed

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