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Enhancing Renal Graft Function During Donor Anesthesia

Renal Graft Functional Enhancement During Donor Anesthesia: A Comparative Study of 3 Modalities

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03778944
Enrollment
60
Registered
2018-12-19
Start date
2018-12-20
Completion date
2026-12-31
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Renal Failure Chronic, Transplant;Failure,Kidney

Keywords

Mannitol, Dopamine, Perfusion, Renal graft donor, Anesthesia

Brief 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.

Interventions

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

PROCEDUREDopamine 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.

PROCEDUREAdequate 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.

Sponsors

Nazmy Edward Seif
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Using computer & sealed envelope randomization, patients are assigned to receive either Mannitol \[M group; n=20\], Dopamine \[D group; n=20\] or adequate hydration \[C group; n=20\]

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* end-stage renal disease, for living-donor kidney transplantation

Exclusion criteria

* severe cardiac or hepatic dysfunction * coagulopathy

Design outcomes

Primary

MeasureTime frameDescription
Post-operative creatinine clearance7 daysPost-operative creatinine clearance level of the transplanted kidney graft is measured in ml/min

Countries

Egypt

Contacts

Primary ContactNazmy E Seif, MD
drnazmyseif@yahoo.com01227400808
Backup ContactAhmed M Elbadawy, MD
elbadawyahmed89@yahoo.com01064249076

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026