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Induction of Drug Metabolism: In Vivo Comparison of Carbamazepine and Oxcarbazepine.
This study is ongoing, but not recruiting participants.
Sponsors and Collaborators: Odense University Hospital
The Danish Research Agency
Novartis
Information provided by: Odense University Hospital
ClinicalTrials.gov Identifier: NCT00260247
  Purpose

This is a study of the possible effect of two antiepileptic drug on enzymes in the liver that metabolizes a number of drugs. It is a well know fact that carbamazepine induces some of these enzymes and this may reduce the effect of concomitantly administered drugs. Clinical observations suggest that oxcarbazepine does not induce these enzymes to the same degree.

This study directly compares the ability of these two drugs to induce the cytochrome P450 3A4 enzyme, in healthy volunteers using a well defined biomarker reaction of a specific enzyme activity.

It is the hypothesis that oxcarbazepine induces CYP3A4 to a lesser degree than carbamazepine.


Condition Intervention Phase
Metabolic Clearance Rate
Drug: carbamazepine oxcarbazepine
Phase IV

Drug Information available for: Carbamazepine Oxcarbazepine Quinidine Quinidine polygalacturonate Quinidine sulfate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Crossover Assignment, Pharmacokinetics Study
Official Title: Induction of Drug Metabolism: A Comparative, Pharmacokinetic in Vivo Study of the Effect of Carbamazepine and Oxcarbazepine on CYP3A4.

Further study details as provided by Odense University Hospital:

Primary Outcome Measures:
  • Formation clearance of 3-hydroxyquinidine

Secondary Outcome Measures:
  • Ratio of metabolite to drug AUC's of 3-OH quinidine to quinidine.

Estimated Enrollment: 10
Study Start Date: April 2005
Estimated Study Completion Date: October 2005
  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • BMI < 30
  • Non smoker
  • No signs or symptoms of disease by routine laboratory analysis, ECG and physical examination (general appearance assessment; pulmonal and cardiac stetoscopy; abdominal palpation)
  • Informed consent

Exclusion Criteria:

  • signs or symptoms of disease by routine laboratory analysis, ECG and physical examination
  • mental disease
  • participation in another clinical trial involving drugs with 3 months of randomization
  • donation of more than 500 mL blood within 3 months of randomization
  • intake of more than 21 alcohol equivanlents (one normal strength beer contain one alcohol equivalent)per week
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00260247

Locations
Denmark
University of Southern Denmark
Odense, Denmark, 5210
Sponsors and Collaborators
Odense University Hospital
The Danish Research Agency
Novartis
Investigators
Principal Investigator: Per Damkier, MD, Ph.D. Odense University Hospital
  More Information

Study ID Numbers: AKF-315
Study First Received: November 28, 2005
Last Updated: November 28, 2005
ClinicalTrials.gov Identifier: NCT00260247  
Health Authority: Denmark: Danish Medicines Agency

Keywords provided by Odense University Hospital:
CYP3A4
Induction
Oxcarbazepine
Carbamazepine
Quinidine
Human
In vivo

Study placed in the following topic categories:
Oxcarbazepine
Carbamazepine
Quinidine

Additional relevant MeSH terms:
Tranquilizing Agents
Physiological Effects of Drugs
Psychotropic Drugs
Central Nervous System Depressants
Antimanic Agents
Pharmacologic Actions
Analgesics, Non-Narcotic
Sensory System Agents
Therapeutic Uses
Analgesics
Peripheral Nervous System Agents
Central Nervous System Agents
Anticonvulsants

ClinicalTrials.gov processed this record on January 14, 2009