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| Sponsor: | Erasme University Hospital |
|---|---|
| Information provided by: | Erasme University Hospital |
| ClinicalTrials.gov Identifier: | NCT00596414 |
Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Cirrhosis Chronic Hepatitis Anxiety |
Procedure: transjugular liver biopsy Drug: placebo Drug: midazolam Drug: midazolam + pethidine |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Single Group Assignment, Efficacy Study |
| Official Title: | Sedation and Analgesia for Transjugular Liver Biopsy: A Randomized Double Blind Placebo Controlled Trial |
| Enrollment: | 180 |
| Study Start Date: | May 2003 |
| Study Completion Date: | October 2005 |
| Primary Completion Date: | October 2005 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| 1: Placebo Comparator |
Procedure: transjugular liver biopsy
liver biopsy through the transjugular route with hepatic-venous pressure gradient measurement
Drug: placebo
|
|
2: Experimental
midazolam
|
Procedure: transjugular liver biopsy
liver biopsy through the transjugular route with hepatic-venous pressure gradient measurement
Drug: midazolam
|
|
3: Experimental
midazolam + pethidine
|
Procedure: transjugular liver biopsy
liver biopsy through the transjugular route with hepatic-venous pressure gradient measurement
Drug: midazolam + pethidine
|
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.
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Responsible Party: | Erasme University Hospital ( Olivier Le Moine, MD, PhD ) |
| Study ID Numbers: | BHTJ-1, BHTJ-1 |
| Study First Received: | January 8, 2008 |
| Last Updated: | January 16, 2008 |
| ClinicalTrials.gov Identifier: | NCT00596414 History of Changes |
| Health Authority: | Belgium: Institutional Review Board |
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liver biopsy |
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Neurotransmitter Agents Liver Diseases Molecular Mechanisms of Pharmacological Action Hepatitis, Chronic Fibrosis GABA Modulators Physiological Effects of Drugs Psychotropic Drugs Anesthetics Meperidine Pathologic Processes Sensory System Agents Therapeutic Uses Hypnotics and Sedatives Analgesics |
Analgesics, Opioid Anesthetics, Intravenous Tranquilizing Agents Central Nervous System Depressants Narcotics Midazolam Pharmacologic Actions Hepatitis Adjuvants, Anesthesia Digestive System Diseases Anesthetics, General GABA Agents Anti-Anxiety Agents Peripheral Nervous System Agents Central Nervous System Agents |