Skip to content

Comparison of Sevoflurane with Propofol based anesthesia technique on echocardiographic strain values in patients undergoing elective aortic valve replacement

Effect of sevoflurane versus propofol on strain quantification in patients with severe aortic stenosis undergoing aortic valve replacement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050850
Enrollment
74
Registered
2023-03-20
Start date
Unknown
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

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Sevoflurane: Sevoflurane based anaesthesia maintenance regimen. Anaesthesia maintenace dose: Sevoflurane inhaled 1 MAC titrated to anesthesia depth bispectral index (BIS) score of 40 -

Sponsors

Markose L Paret
Lead Sponsor
SCTIMST
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All adults above 18 years of age, in sinus rhythm, admitted with severe aortic stenosis with good LV function (Left ventricular ejection fraction more than or equal to 50%) for elective aortic valve replacement surgery will be included in the study

Exclusion criteria

Exclusion criteria: 1. Emergency surgeries 2. Redo surgeries 3. Patients not willing to participate in study 4. More than mild AR, MR or TR 5. Patients with coronary artery disease defined by lumen stenosis more than or equal to 50% in atleast one of major epicardial coronaries on coronary angiogram. 6. Patients receiving preoperative inotropes 7. Patients with poor echo differentiation of endocardial borders 8. Contraindication to TEE probe placement like esophageal strictures, esophageal varices, esophageal tumours, gastric ulcer, previous esophagectomy, esophageal diverticulum, tracheoesophageal fistula, previous bariatric surgery, hiatus hernia, large descending thoracic aortic aneurysm, unilateral vocal cord paralysis, esophageal varices, post-radiation therapy

Design outcomes

Primary

MeasureTime frame
1. Change in global longitudinal and global circumferential strain after aortic valve replacement in patients of severe aortic stenosis with good left ventricular ejection fraction 2. Compare effects of sevoflurane and propofol anaesthesia on changes in global longitudinal and circumferential strain after aortic valve replacement in patients of severe aortic stenosis with good left ventricular ejection fraction. Timepoint: 1. Strain echocardiography before aortic valve replacement in intraoperative period. 2. Strain echocardiography after aortic valve replacement in intraoperative period

Secondary

MeasureTime frame
1. Assess preoperative global longitudinal and circumferential strains in patients with severe aortic stenosis and good left ventricular ejection fraction. 2. To study risk factors associated with preoperative changes in global longitudinal and circumferential strain in patients with severe aortic stenosis and good left ventricular ejection fraction. Timepoint: 1.Risk factor evaluation during preoperative anaesthesia check up. 2. Strain echocardiography before aortic valve replacement in intra operative period. 3.Strain echocardiography after aortic valve replacement in intraoperative period.

Countries

India

Contacts

Public ContactMarkose L Paret

SCTIMST

shri@sctimst.ac.in9446304043

Outcome results

None listed

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