Observing factors causing right side heart dysfunction in patient with acute respiratory failure
Not Applicable
- Conditions
- Health Condition 1: J22- Unspecified acute lower respiratory infection
- Registration Number
- CTRI/2021/03/032207
- Lead Sponsor
- Department of anesthesia and intensive care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
study will be conducted between march 2021 and december 2021 after clearance from Institutional Ethics Committee. All patients between the ages of 18 years to 75 years with moderate to severe ARDS based on Berlin definition criteria will be included in this trial.
Exclusion Criteria
1.Patients with prior history of RV dysfunction or pulmonary hypertension
2.Patient or guardian refusal to participate in this study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method prospective observational study to evaluate the impact of clinical parameters, demographic and etiological factors on right ventricle dysfunction in patient with ARDSTimepoint: Assessed at time of admission in ICU and every week for 4 weeks and at discharge
- Secondary Outcome Measures
Name Time Method To find incidence of RV dysfunction in ARDSTimepoint: Till ICU stay or upto 28 days;To study the impact of RV dysfunction on outcome in ARDS patient during the course of illness.Timepoint: till ICU stay or 28 days