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NCT02019121 Clinical Trial

Dexmedetomidine and Renal Transplants

Renal Failure Clinical Trial

Official title:
Dexmedetomidine and Renal Transplants

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02019121
Other study ID # 521455
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2013
Est. completion date February 2020

Study information
Verified date July 2022
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 797
Est. completion date February 2020
Est. primary completion date February 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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. -

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States UC Davis Health System Sacramento California

Sponsors (1)
Lead Sponsor Collaborator
University of California, Davis

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Other length of intubation time, and length of ventilation time 5 years
Primary Cr/GFR improvement, postoperative mortality/morbidity (within 30 days) and overall complications 5 years
Secondary Graft failure, length of hospital stay (LOS), length of ICU stay, re-admission rate, infections, pulmonary complications. 5 years
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