Skip to main content
OpenTrials
Completed

NCT Number: NCT01104337

Drug Interaction Between Paracetamol and Warfarin

The objective of this study is to investigate whether paracetamol, given at therapeutic doses (2g/day and 3 g/day), may potentiate the anticoagulant effect of warfarin.

Completed

Looking for future studies?

Notify Me

Key information

About this study

Paracetamol is recommended as a first-line analgesic and antipyretic therapy in patients receiving short- and long-term oral anticoagulation, especially elderly patient.However,Increased INR was previously observed in patients treated with warfarin and paracetamol given at the maximum recommended dose (4g/day).

To date, the mechanism of this interaction has not been determined.A recent in vitro study suggested that the toxic metabolite N-acetyl-para-benzoquinoneimine (NAPQI) appeared to interfere with vitamin K-dependent γ-carboxylase (VKD-carb) and vitamin K epoxide reductase (VKOR) activites12. The question remaining to be dealt with is whether this in vitro observation can explain the in vivo paracetamol-warfarin interaction. We aim to evaluate the effect of paracetamol at the most widely used doses 2 and 3g/day on INR in stable patients treated with warfarin in a double blind randomized placebo-controlled trial and to identify the mechanism involved in this interaction in vivo.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients treated with warfarin (target INR 2 to 3) stable anticoagulation at 2 to 9 mg for more than 30 days
  • Aged 18 years or older
  • Laboratory values (hemoglobin, blood cell counts, albumin, blood ionogram, complementary hemostasis parameters and aspartate, alanine transaminases (AST and ALT))remained within normal limits

Exclusion criteria

  • Any treatment change within 7 days before enrollment
  • Any paracetamol intake within the last 14 days
  • Drug allergy Concomitant drug ( 5-fluorouracile, acetylsalicylic acid, non steroidal anti-inflammatory drugs, chloramphenicol, diflunisal, miconazole)
  • St John's wort treatment
  • Pregnancy

Treatment and study plan

Paracetamol

Drug

Treatment consisted of two paracetamol 500mg (Doliprane® 500mg, Sanofi-aventis, Paris, France) tablets twice a day along with two matching placebo tablets once daily

Placebo

Drug

Treatment consisted of two matching placebo tablets three times a day.

Primary outcomes

  1. The mean maximum increase in INR from baseline to Day 10 (INR (max-D1))

    Time frame: 10 days

Secondary outcomes

  1. The mean maximum INR (INRmax)

    Time frame: 10 days

  2. The time to the first variation of INR observed

    Time frame: 10 days

  3. Day 10 - Day 1 differences in factors II, V, VII, AT-III plasma concentrations between groups.

    Time frame: 10 days

  4. Day 10 - Day 1 differences in paracetamol plasma concentration between groups.

    Time frame: 10 days

  5. Day 10 - Day 1 differences in R(-), S(-)warfarin plasma concentrations between groups.

    Time frame: 10 days

  6. Day 10 - Day 1 differences in Gla-type Osteocalcin (Gla-OC) and undercarboxylated Osteocalcin (Glu-OC)plasma concentrations between groups.

    Time frame: 10 days

  7. Relation between age and the mean maximum increase in INR from baseline to Day 10 (INR (max-D1)

    Time frame: 10 days

    Relation between age and INR (max-D1)is measured using regression analysis.

Sponsors and collaborators

Lead sponsor

Hopital Lariboisière

Other

Registry information

Official study title

Dose-dependent Drug-drug Interaction Between Paracetamol and Warfarin in Adults Receiving Long-term Oral Anticoagulants: A Randomized Controlled Trial

Acronym: INPAWA2

Important dates

Study start
2007
Primary completion
2008
Study completion
2010
First posted
Apr 15, 2010
Registry last updated
Apr 15, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.