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Changes in Heart Filling Function Before and After Ventilator Support During Heart Surgery

Assessment of left ventricular Diastolic Function in Spontaneously Breathing Patient and Patient on Mechanical Ventilation Undergoing Cardiac Surgeries - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/112411
Enrollment
103
Registered
2026-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: I259- Chronic ischemic heart disease, unspecified

Interventions

Intervention1: Nil: Nil

Sponsors

Postgraduate Institute of Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adult patients above 18 years scheduled for elective, isolated CABG and AVR for aortic stenosis. 2.Ability to provide informed consent. 3.Feasibility of obtaining technically adequate Transthoracic Echocardiography (TTE) windows at both T1 and T2 time points.

Exclusion criteria

Exclusion criteria: 1.Emergency/Salvage cardiac surgery. 2.Prior history of cardiac surgery (to avoid complex confounding of ventricular geometry). 3.Pre-existing severe primary valvular heart disease (other than the indication for AVR). 4.Technical inability to perform adequate TTE at either T1 or T2. Need for immediate post-intubation hemodynamic support that prevents the 15-minute T2 assessment

Design outcomes

Primary

MeasureTime frame
To find the agreement of peak early diastolic mitral annular velocity (lateral e ) and. (Medial e ) measured by TTE Awake and TTE Mechanically ventilatedTimepoint: T1 (Baseline): Before induction of anaesthesia while the patient is breathing spontaneously T2: Fifteen minutes after intubation and initiation of mechanical ventilation, after hemodynamic stabilization

Secondary

MeasureTime frame
Change in TR velocity & estimated PASP between T1 & T2Timepoint: Baseline / T1: Pre-induction, while the patient is awake & breathing spontaneously T2: Fifteen minutes after endotracheal intubation & initiation of mechanical ventilation, after hemodynamic stabilization & before surgical incision;Change in pulmonary venous S, D, & S/D ratio between T1 & T2Timepoint: Baseline / T1: Pre-induction, while the patient is awake & breathing spontaneously T2: Fifteen minutes after endotracheal intubation & initiation of mechanical ventilation, after hemodynamic stabilization & before surgical incision;Identification of diastolic parameters most & least affected by positive pressure ventilationTimepoint: Baseline / T1: Pre-induction, while the patient is awake & breathing spontaneously T2: Fifteen minutes after endotracheal intubation & initiation of mechanical ventilation, after hemodynamic stabilization & before surgical incision;Proportion of patients with reclassification of LV diastolic dysfunction grade between T1 & T2Timepoint: Baseline / T1: Pre-induction, while the patient is awake & breathing spontaneously T2: Fifteen minutes after endotracheal intubation & initiation of mechanical ventilation, after hemodynamic stabilization & before surgical incision;Predictors of LVDD grade discordance between T1 & T2Timepoint: Baseline / T1: Pre-induction, while the patient is awake & breathing spontaneously T2: Fifteen minutes after endotracheal intubation & initiation of mechanical ventilation, after hemodynamic stabilization & before surgical incision;Association of LVDD grades with duration of mechanical ventilationTimepoint: From postoperative ICU admission until successful extubation / discontinuation of mechanical ventilation.;Association of LVDD grades with ICU length of stayTimepoint: From postoperative ICU admission until ICU discharge.;Association of LVDD grades with need for inotropic or vasopressor supportTimepoint: From postoperative ICU admission until discon

Countries

India

Contacts

Public ContactDr Sunder Lal Negi

Postgraduate Institute of Medical Education and Research

dr.sundernegi@gmail.com9888446388

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026