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Non-invasive Evaluation of the Predictive Value of CEUS and SWE in ACLF, Renal Failure and Hepatorenal Syndrome (NECTAR)

U

University Hospital Bonn (UKB)

Status

Enrolling

Conditions

Kidney Failure, Acute

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Evaluation of non-invasive prognostic parameters in patients developing ACLF and renal failure in patients receiving and not receiving transjugular intrahepatic portosystemic shunt (TIPS). Patients are cared according to the local standardized follow up program. Clinical and laboratory data from standard patient care are evaluated for potential prognostic value.

Full description

NECTAR consists of patients with ACLF and renal failure with and without receiving transjugular intrahepatic portosystemic shunt (TIPS) at the Department of Internal Medicine I, University of Bonn, Germany and receiving a structured routine evaluation and follow up program. The diagnosis of cirrhosis was based on clinical, hemodynamic and biochemical parameters, and ultrasound and/or biopsy criteria.

Enrollment

1,000 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients with portal hypertension and kidney failure

Exclusion criteria

  • no consent, no kidney failure, no portal hypertension

Trial design

1,000 participants in 2 patient groups

With TIPS
Description:
Prospective cohort that received TIPS
Without TIPS
Description:
Prospective cohort that did not receive TIPS

Trial contacts and locations

1

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Central trial contact

Johannes Chang, MD; Michael Praktiknjo, MD

Data sourced from clinicaltrials.gov

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