Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
ID03071536

Furosemide Stress Test as a Marker of Postoperative Kidney Allograft Function

Led by King Chulalongkorn Memorial Hospital · Updated on 2024-01-17

180

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the response to a standardized dose of furosemide in patients who have undergone kidney transplantation. The study focuses on measuring urine output after administering furosemide as a way to predict early kidney graft function in the perioperative period. This approach addresses a gap, as no previous study has directly assessed urine response to a standardized furosemide dose post-transplant. Participants receive a single intravenous dose of furosemide at 1.5 mg/kg three hours after the kidney allograft is reperfused. Urine output is then recorded hourly for six hours following the dose. This intervention is assessed as an experimental approach to understand its role as a biomarker for kidney function after transplantation. Throughout the study, urine output is closely monitored for six hours after furosemide administration, and additional outcomes such as delayed graft function over seven days and creatinine reduction ratio on postoperative days 0, 7, and 14 are evaluated. The study involves follow-up assessments to track kidney function and graft performance, providing important data on early postoperative kidney health. Participants remain under observation to measure these outcomes until the study concludes.

CONDITIONS

Brief Title

Furosemide Stress Test Predicting Early Graft Function in Kidney Transplantation

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Deceased donor kidney transplantation at King Chulalongkorn Memorial Hospital
  • Informed consent is accepted
  • Age between 18 and 80 years
Not Eligible

You will not qualify if you...

  • Known allergy to furosemide
  • Surgical complication of allograft
  • Urgently needed for dialysis due to refractory hypervolemia, uremic symptoms, or hyperkalemia

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 hours

Participants receive a single intravenous dose of furosemide 3 hours after kidney transplant reperfusion. Urine output is recorded hourly for 6 hours following the dose.

1 treatment visit with hourly monitoring for 6 hours

Follow-up

Duration - 14 days

Participants are monitored postoperatively with assessments of graft function and kidney health up to 14 days after transplant.

Visits at postoperative day 0, 7, and 14

Trial Site Locations

Total: 1 location

1

King Chulalongkorn Memorial Hospital

Bangkok, Thailand, 10330

Actively Recruiting

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Research Team

S

Suwasin udomkarnjananun, M.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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Published Research Related To This Trial

Furosemide Stress Test as a Predicting Biomarker for Delayed Graft Function in Kidney Transplantation.

Suwasin Udomkarnjananun, Natavudh Townamchai, Kroonpong Iampenkhae...

https://pubmed.ncbi.nlm.nih.gov/30636249