Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
ID03778944

Renal Graft Functional Enhancement During Donor Anesthesia: Comparing Mannitol, Dopamine, and Hydration Treatments

Led by Nazmy Edward Seif · Updated on 2026-01-12

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Renal transplantation is recognized as the preferred treatment for patients with end-stage renal disease. This research aims to compare the effects of three different treatments given during donor anesthesia to improve the function and blood flow of the transplanted kidney. The study focuses on assessing how Mannitol, Dopamine, and adequate hydration each impact kidney function after surgery. Participants will receive one of three treatments during anesthesia for kidney donation: a Mannitol infusion at 0.5 mg/kg over 15 minutes after anesthesia induction; a Dopamine infusion at 4 microg/kg/min from anesthesia induction until the renal artery is tied off; or adequate hydration via Ringer Acetate at 15 ml/kg/hr during the same period. These different approaches are being studied to find which best supports the transplanted kidney. During the study, researchers will monitor kidney function by measuring creatinine clearance seven days after surgery. Participants will be randomly assigned to one of the three treatment groups, and the study is single-blinded. The trial began in December 2018 and is expected to continue until December 2026. Adults aged 18 to 60 with end-stage renal disease who are living-kidney donors will be involved, with careful follow-up to compare outcomes across the treatment methods.

CONDITIONS

Brief Title

Enhancing Renal Graft Function During Donor Anesthesia

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 60 years
  • Diagnosed with end-stage renal disease
  • Scheduled for living-donor kidney transplantation
Not Eligible

You will not qualify if you...

  • Severe cardiac dysfunction
  • Severe hepatic dysfunction
  • Coagulopathy (bleeding disorders)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Duration of donor anesthesia until renal artery ligation

Participants receive one of three interventions during donor anesthesia: Mannitol infusion over 15 minutes, Dopamine infusion until renal artery ligation, or adequate hydration until renal artery ligation.

1 treatment visit during surgery

Post-operative Follow-up

Duration - 7 days

Participants are monitored for kidney function after surgery.

Approximately 1 follow-up visit

Trial Site Locations

Total: 1 location

1

Kasr Al-Ainy Hospital, Cairo University

Cairo, Egypt

Actively Recruiting

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Research Team

N

Nazmy E Seif, MD

A

Ahmed M Elbadawy, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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