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Accuracy of the USCOM in monitoring of hemodynamic status during renal transplantation.

Accuracy of the USCOM ultrasonic cardiac output monitor for intraoperative hemodynamic monitoring in renal transplant recipients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/03/050649
Enrollment
100
Registered
2023-03-13
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: N186- End stage renal disease

Interventions

Control Intervention1: Nil: Nil Control Intervention2: Nil: Nil

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with chronic kidney disease Stage 5, scheduled for elective renal transplant surgery will be included.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.—

Countries

India

Contacts

Public ContactKamal Kajal

Postgraduate Institute of Medical Education and Research, Chandigarh

kamal.kajal@gmail.com

Outcome results

None listed

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