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Dexmedetomidine and Renal Transplants

Dexmedetomidine and Renal Transplants

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02019121
Enrollment
797
Registered
2013-12-24
Start date
2013-10-31
Completion date
2020-02-29
Last updated
2022-07-11

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

Conditions

Renal Failure

Brief summary

Investigators aim to retrospectively research patients undergoing renal transplants that received dexmedetomidine perioperatively to see if dexmedetomidine use protects renal function. Investigators hope to elucidate any association between renal transplant patients and perioperative dexmedetomidine administration, these include (but are not limited to) UOP, Cr/GFR, morbidity, mortality, in hospital complications and failure rate. Investigators will research both living and cadaveric renal transplants.

Interventions

None listed

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

Patients greater than or equal to 18 years old that underwent renal transplant at UC Davis Medical Center -

Exclusion criteria

Patients that did not undergo renal transplants and patients less than 18 years old will be excluded from the study. \-

Design outcomes

Primary

MeasureTime frame
Cr/GFR improvement, postoperative mortality/morbidity (within 30 days) and overall complications5 years

Secondary

MeasureTime frame
Graft failure, length of hospital stay (LOS), length of ICU stay, re-admission rate, infections, pulmonary complications.5 years

Other

MeasureTime frame
length of intubation time, and length of ventilation time5 years

Countries

United States

Outcome results

None listed

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