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Relationship Between Folic Acid and Warfarin Metabolism and Effect
This study is currently recruiting participants.
Verified by Hadassah Medical Organization, October 2008
Sponsored by: Hadassah Medical Organization
Information provided by: Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT00162409
  Purpose

Folic acid supplementation has been shown previously to be associated with enhanced formation of p-HPPH from phenytoin, a metabolic pathway which is predominantly mediated through the activity of CYP2C9.

The metabolism of S warfarin, the more active enantiomer of warfarin, is also mediated predominantly through the activity of CYP2C9.

The purpose of the present study was to examine the relationship between folic acid concentration and warfarin pharmacokinetic as well as warfarin dose requirement among patients treated by warfarin. In addition the effect of folic acid supplementation (5 mg/d) for 3 weeks on warfarin pharmacokinetic and warfarin dose requirement will be evaluated in the second part of the study.


Condition Intervention
Folic Acid Deficiency
Drug: Folic acid

MedlinePlus related topics: Blood Thinners
Drug Information available for: Folic acid Warfarin Warfarin potassium Warfarin sodium
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Pharmacokinetics/Dynamics Study
Official Title: The Effect of Folic Acid Concentration and Folic Acid Supplementation on Warfarin Pharmacokinetic and Warfarin Dose Requirement at Steady State.

Further study details as provided by Hadassah Medical Organization:

Primary Outcome Measures:
  • Warfarin pharmacokinetic prior to and following administration of folic acid
  • Warfarin dose requirement prior to and following the administration of folic acid.

Estimated Enrollment: 400
Study Start Date: August 2001
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients on chronic warfarin therapy

Exclusion Criteria:

  • Refusal to participate in the study
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00162409

Contacts
Contact: Yoseph Caraco, MD 00 972 2 6778584 caraco@hadassah.org.il

Locations
Israel
Hadassah Medical Organization Recruiting
Jerusalem, Israel
Contact: Arik Tzukert, DMD     00 972 2 6776095     arik@hadassah.org.il    
Contact: Hadas Lemberg, PhD     00 972 2 6777572     lhadas@hadassah.org.il    
Principal Investigator: Yoseph Caraco, MD            
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Yoseph Caraco, MD Hadassah Medical Organization
  More Information

Study ID Numbers: yc19552-HMO-CTIL
Study First Received: September 11, 2005
Last Updated: October 28, 2008
ClinicalTrials.gov Identifier: NCT00162409  
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Study placed in the following topic categories:
Folic Acid
Malnutrition
Avitaminosis
Folic Acid Deficiency
Nutrition Disorders
Warfarin
Deficiency Diseases

Additional relevant MeSH terms:
Anticoagulants
Vitamin B Complex
Vitamin B Deficiency
Hematinics
Therapeutic Uses
Growth Substances
Vitamins
Hematologic Agents
Physiological Effects of Drugs
Micronutrients
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 15, 2009