Clinical Trials in Egypt / NCT03778944
Recruiting Not applicable

Enhancing Renal Graft Function During Donor Anesthesia

NCT03778944 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2018-12-20
Last updated
2026-01-12

Condition(s) studied

Renal Failure ChronicTransplant;Failure,KidneyAnesthesia

Investigational drug(s) / intervention(s)

Mannitol infusionDopamine infusionAdequate hydration

Mannitol infusion: Infusion of Mannitol 20% at a dose of 0.5 mg/kg to the renal graft donor after induction of anesthesia over 15 minutes.

Dopamine infusion: Infusion of Dopamine at a dose of 4 microg/kg/min to the renal graft donor after induction of anesthesia till ligation of the renal artery.

Adequate hydration: Infusion of Ringer Acetate at a rate of 15 ml/kg/hr to the renal graft donor after induction of anesthesia till ligation of the renal artery.

Study summary

Renal transplantation is now recognized as the treatment of choice for patients with end-stage renal disease. An optimum anesthetic regimen should enhance the function and perfusion of the transplanted kidney. The aim of this study is to assess \& compare the effectiveness of 3 different modalities in this respect: Mannitol, Dopamine and adequate hydration.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * end-stage renal disease, for living-donor kidney transplantation Exclusion Criteria: * severe cardiac or hepatic dysfunction * coagulopathy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kasr Al-Ainy Hospital, Cairo University Cairo Egypt Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03778944 on ClinicalTrials.gov ↗ ← All trials in Egypt