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BK Virus and Renal Dysfunction in Postoperative/Posttraumatic Critically Ill Patients (BICUK)

U

University of Ulm

Status

Completed

Conditions

Multiple Organ Dysfunction Syndrome
SIRS
Critically Ill
Acute Renal Failure
Sepsis

Study type

Observational

Funder types

Other

Identifiers

NCT00736827
Anae_ICU_Ulm_BKV

Details and patient eligibility

About

The purpose of this study is to find out whether acute renal failure is associated with BK virus reactivation in postoperative/posttraumatic critically ill patients with severe SIRS/sepsis and shock.

Full description

Polyomavirus BK virus (BKV) infection and nephropathy is a significant cause of allograft dysfunction in kidney transplantation. Clinical manifestation ranges from BK viremia and nephritis to renal dysfunction. It has been suggested that BK virus reactivation alone is not sufficient to cause BK viremia and nephropathy, thus a second hit is essential for kidney specific damage, such as an inflammatory reaction or ischemia. Critically ill postoperative/posttraumatic patients via the systemic inflammatory response syndrome (SIRS) and the compensatory antiinflammatory response syndrome (CARS) are at increased risk to develop organ dysfunctions, such as acute renal failure. CARS, reflecting postoperative/posttraumatic immunosuppression, may favor viral reactivation. However, prevalence of BK viremia in critically ill postoperative/posttraumatic patients has up to now not been systematically evaluated. Moreover, it is not known whether BK viremia is associated with a distinct biomarker pattern in these patients. Therefore, the present study is performed to clarify whether postoperative/posttraumatic immunosuppression is associated with BK viremia, and acute renal failure with BK virus reactivation, respectively.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Critically ill, postoperative/posttraumatic patients with threatening acute renal failure

Exclusion criteria

  • Life expectancy < 24 hours
  • Participation in other trials
  • Known or suspected pregnancy

Trial design

51 participants in 2 patient groups

Patients with non-septic shock
Description:
Postoperative/posttraumatic surgical critically ill patients with non-septic shock with threatening acute renal failure
Patients with septic shock
Description:
Postoperative/posttraumatic surgical critically ill patients with septic shock with threatening acute renal failure

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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