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Clinical Trials/NCT03778944
NCT03778944RecruitingNot Applicable

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

Nazmy Edward Seif1 site in 1 country60 target enrollmentStarted: December 20, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Post-operative creatinine clearance

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

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

Exclusion Criteria

  • •severe cardiac or hepatic dysfunction
  • •coagulopathy

Arms & Interventions

C group

Active Comparator

Adequate hydration

Intervention: Adequate hydration (Procedure)

M group

Active Comparator

Mannitol infusion

Intervention: Mannitol infusion (Procedure)

D group

Active Comparator

Dopamine infusion

Intervention: Dopamine infusion (Procedure)

Outcomes

Primary Outcomes

Post-operative creatinine clearance

Time Frame: 7 days

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Nazmy Edward Seif
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Nazmy Edward Seif

Clinical Professor

Cairo University

Study Sites (1)

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