Accuracy of the USCOM in monitoring of hemodynamic status during renal transplantation.
Not Applicable
- Conditions
- Health Condition 1: N186- End stage renal disease
- Registration Number
- CTRI/2023/03/050649
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with chronic kidney disease Stage 5, scheduled for elective renal transplant surgery will be included.
Exclusion Criteria
Age <18 yrs, congenital heart disease, patients with pulmonary edema, emphysema, chest wall deformities, morbid obesity, lack of consent, aortic regurgitation, severe hypovolemia, arrhythmias, and poor echo window.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Agreement between the USCOM and TTE for the measurement of CO in patients undergoing renal transplant.Timepoint: Pre-induction, 5 minutes post-induction, 1 hour post-induction, 5 minutes post-reperfusion, during closure of abdomen.
- Secondary Outcome Measures
Name Time Method To study the hemodynamic changes during the intraoperative course of renal transplant surgeryTimepoint: Pre-induction, 5 minutes post-induction, 1 hour post-induction, 5 minutes post-reperfusion, during closure of abdomen.