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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00596414
Other study ID # BHTJ-1
Secondary ID BHTJ-1
Status Completed
Phase Phase 4
First received January 8, 2008
Last updated January 16, 2008
Start date May 2003
Est. completion date October 2005

Study information

Verified date December 2007
Source Erasme University Hospital
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Transjugular liver catheterisation allows the measurement of hepatic venous pressure gradient (HVPG) and the sampling of liver tissue but patient's tolerance to the procedure is unknown. The aim of this study was to assess tolerance to transjugular hepatic liver biopsy with or without conscious sedation/analgesia.


Description:

Consecutive patients undergoing transjugular liver biopsy will be randomly assigned to receive either placebo or midazolam (0.02 mg/kg) or 0.02 mg/kg midazolam combined with 1 mg/kg pethidine before the procedure.


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date October 2005
Est. primary completion date October 2005
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- suspected liver disease

- known liver disease

Exclusion Criteria:

- liver transplants

- hepatocellular carcinoma

- hypersensitivity or allergy to benzodiazepines or morphinic derivatives

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
transjugular liver biopsy
liver biopsy through the transjugular route with hepatic-venous pressure gradient measurement
Drug:
placebo

midazolam

midazolam + pethidine


Locations

Country Name City State
Belgium Hopital Erasme - Dpt of Gastroenterology Brussels

Sponsors (1)

Lead Sponsor Collaborator
Erasme University Hospital

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient tolerance to the procedure 1 hour after the procedure Yes
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