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4beta-hydroxycholesterol in Cirrhosis

U

University of Oulu

Status

Suspended

Conditions

Cirrhosis, Liver

Treatments

Other: There is no intervention, only research blood samples are collected

Study type

Observational

Funder types

Other

Identifiers

NCT04199910
4bHC kirroosissa

Details and patient eligibility

About

The aim is to evaluate the levels of oxysterols and especially 4beta-hydroxycholesterol in patients with liver cirrhosis. Three cirrhosis cohorts are recruited: patients treated with spironolactone, patients treated with rifaximin, patients without spironolactone or rifaximin. Also three other control cohorts are recruited: patients with pneumonia, patients with Crohn's disease, patients with ulcerative colitis. The effect of the cirrhosis and its medications spironolactone and rifaximin are compared to control groups.

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with cirrhosis, pneumonia, Crohn's disease or colitis ulcerosa
  • Treated in the ward 42 of the Oulu University Hospital

Exclusion criteria

  • None

Trial design

120 participants in 6 patient groups

Liver cirrhosis with spironolactone
Treatment:
Other: There is no intervention, only research blood samples are collected
Liver cirrhosis with rifaximin
Treatment:
Other: There is no intervention, only research blood samples are collected
Liver cirrhosis without spironolactone or rifaximin
Treatment:
Other: There is no intervention, only research blood samples are collected
Pneumonia
Treatment:
Other: There is no intervention, only research blood samples are collected
Crohn's disease
Treatment:
Other: There is no intervention, only research blood samples are collected
Ulcerative colitis
Treatment:
Other: There is no intervention, only research blood samples are collected

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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