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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01782209
Other study ID # DMID 11-0071
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2014
Est. completion date December 2019

Study information

Verified date July 2020
Source University of Alabama at Birmingham
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objectives of this study is to establish the natural history of BK virus viremia and other possible opportunistic viral pathogens in renal transplants recipients.


Description:

This is a Natural History study in renal or renal-pancreas transplant recipients. In an effort to capture patients early in the course of an evolving BK virus infection and avoid patients who have already developed evidence of BKV-induced nephropathy (BKVN), this protocol will emphasize the initiation of screening in the early post-transplant period. Patients who have undergone renal or renal/pancreas transplantation within 4 weeks, but not more than 90 day previously, will be asked to participate and then consented to be enrolled in a Natural History-Surveillance period for up to approximately 24 months. Participants enrolled in this study will provide valuable natural history data regarding BKV viremia, and potentially other viral pathogen, in the post-renal transplant period. Participants will provide blood samples to undergo measurement for plasma BKV DNA by PCR approximately every 6 weeks, to be resulted in real time at the UAB Diagnostic Virology Laboratory at UAB.


Recruitment information / eligibility

Status Completed
Enrollment 335
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Renal or renal-pancreas transplant patients who are within 4 weeks and not more than 90 days post-transplant with or without qualifying BKV viremia Age greater than or equal to 18 years; Provides written informed consent.

Exclusion Criteria:

Evidence of proven or suspected BKVN by clinical or pathologic diagnostic criteria Loss of renal graft function Initiation of chronic dialysis

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Alabama at Birmingham Birmingham Alabama
United States University of Colorado at Denver and HSC Denver Colorado
United States University of Minnesota Minneapolis Minnesota
United States Columbia University New York New York
United States Washington University, Barnes Jewish Hospital Saint Louis Missouri
United States California Pacific Medical Center San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of BKV Viremia in the Study Population of Screened Renal or Renal-pancreas Transplant Subjects We will measure the number of subjects screened who develops BK viremia within 4 weeks and up to 24 months after renal transplant within 4 weeks and up to 24 months after renal transplant