Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 60 years
- Diagnosed with end-stage renal disease
- Scheduled for living-donor kidney transplantation
You will not qualify if you...
- Severe cardiac dysfunction
- Severe hepatic dysfunction
- Coagulopathy (bleeding disorders)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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
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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