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Study to Find Out the Appropriate Initial Dose of the Anticoagulant Drug Phenprocoumon

Primary Purpose

Pulmonary Embolism, Atrial Fibrillation, Hip Replacement Postoperative

Status
Completed
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Algorithm for phenprocoumon
algorithm for phenprocoumon
Phenprocoumon
Sponsored by
Cantonal Hospital of St. Gallen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Embolism focused on measuring Phenprocoumon, Dosing algorithm, loading dose

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Consecutive inpatients of the internal medicine and the orthopedic surgery department of the Cantonal Hospital of St. Gallen needing new onset oral anticoagulation

Exclusion Criteria:

  • Patients with prior oral anticoagulation with coumarines within less than 6 weeks,
  • patents, who received vitamin-K supplements within less than one week before the onset of oral anticoagulation,
  • patients with liver cirrhosis other than Child A,
  • pregnant women (pregnancy has to be excluded in women of childbearing age),
  • patients younger than 18 years, and
  • patients unwilling or unable to give informed consent
  • patients with (clinically diagnosed) dementia and
  • persons with insufficient German, French, Italian or English language skills)

Sites / Locations

  • Cantonal Hospital St. Gallen

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

A

B

C

Arm Description

Algorithm which uses serum albumin and weight to determine the loading dose of phenprocoumon within the first 5 days

Algorithm which uses serum age and weight to determine the loading dose of phenprocoumon within the first 5 days

The physician chooses the loading dose of phenprocoumon according to his/her experience

Outcomes

Primary Outcome Measures

rate of patients with therapeutic INR levels on day six without anticoagulation-related complications during the loading period

Secondary Outcome Measures

the time-course of the INR-values, the rate of excessive INR-values, defined as INR >3.5 within 10 days, the rate of minor and major bleeding complications, the length of stay, and death within 30 days

Full Information

First Posted
December 20, 2007
Last Updated
March 29, 2012
Sponsor
Cantonal Hospital of St. Gallen
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1. Study Identification

Unique Protocol Identification Number
NCT00586287
Brief Title
Study to Find Out the Appropriate Initial Dose of the Anticoagulant Drug Phenprocoumon
Official Title
Prospective Randomized Trial of a Clinical Algorithm to Predict the Loading Dose of Phenprocoumon
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
December 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cantonal Hospital of St. Gallen

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Oral anticoagulation is often initiated in hospitalized patients. Although the therapeutic range of phenprocoumon is narrow, the individual drug demands unfortunately vary greatly between persons. Our group recently developed two dosing algorithms for the initiation of anticoagulation based on clinical predictors such as age, gender, body weight and laboratory values. The aim of the proposed study is to prospectively evaluate the efficacy and safety of these two algorithms in medical and orthopedic inpatients, as well as in a group of outpatients and possibly in a geriatric collective.
Detailed Description
Background: The presently available oral anticoagulants have a very narrow therapeutic range but the interindividual demands to achieve therapeutic anticoagulation (=loading dose) varies greatly. Overanticoagulation is a major cause of bleeding complications, whereas insufficient anticoagulation is associated with thromboembolic disease and possibly prolonged hospital stay. A model to predict the loading dose with phenprocoumon (Marcoumar®) is therefore highly desirable. In a retrospective analysis of 300 inpatients (152 medical, 148 orthopedic patients) of the Cantonal Hospital of St. Gallen our group identified clinical predictors for the loading dose of phenprocoumon and two dosing algorithms were developed (Good AC, Henz S. A clinical algorithm to predict the loading dose of phenprocoumon. Thromb Res. 2007;120(6):921-5.). In order to validate the safety and efficacy of these dosing algorithms we plan this prospective interventional study with three equally sized arms: dosing according to algorithm 1, dosing according to algorithm 2 or dosing according to the estimate of the physician (control).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Embolism, Atrial Fibrillation, Hip Replacement Postoperative, Knee Replacement Postoperative
Keywords
Phenprocoumon, Dosing algorithm, loading dose

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
302 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Algorithm which uses serum albumin and weight to determine the loading dose of phenprocoumon within the first 5 days
Arm Title
B
Arm Type
Experimental
Arm Description
Algorithm which uses serum age and weight to determine the loading dose of phenprocoumon within the first 5 days
Arm Title
C
Arm Type
Active Comparator
Arm Description
The physician chooses the loading dose of phenprocoumon according to his/her experience
Intervention Type
Other
Intervention Name(s)
Algorithm for phenprocoumon
Other Intervention Name(s)
Marcoumar
Intervention Description
Dosing of phenprocoumon for days 1 to 3, measuring INR and adjust dose according algorithm A published in (Good AC, Henz S. A clinical algorithm to predict the loading dose of phenprocoumon. Thromb Res. 2007;120(6):921-5.)
Intervention Type
Other
Intervention Name(s)
algorithm for phenprocoumon
Other Intervention Name(s)
Marcoumar
Intervention Description
Dosing of phenprocoumon for days 1 to 3, measuring INR and adjust dose according algorithm B published in (Good AC, Henz S. A clinical algorithm to predict the loading dose of phenprocoumon. Thromb Res. 2007;120(6):921-5.)
Intervention Type
Drug
Intervention Name(s)
Phenprocoumon
Other Intervention Name(s)
Marcoumar
Intervention Description
Dosing of phenprocoumon for days 1 to 3, measuring INR and adjust dose according to the discretion of the treating physician
Primary Outcome Measure Information:
Title
rate of patients with therapeutic INR levels on day six without anticoagulation-related complications during the loading period
Time Frame
after 30 days
Secondary Outcome Measure Information:
Title
the time-course of the INR-values, the rate of excessive INR-values, defined as INR >3.5 within 10 days, the rate of minor and major bleeding complications, the length of stay, and death within 30 days
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Consecutive inpatients of the internal medicine and the orthopedic surgery department of the Cantonal Hospital of St. Gallen needing new onset oral anticoagulation Exclusion Criteria: Patients with prior oral anticoagulation with coumarines within less than 6 weeks, patents, who received vitamin-K supplements within less than one week before the onset of oral anticoagulation, patients with liver cirrhosis other than Child A, pregnant women (pregnancy has to be excluded in women of childbearing age), patients younger than 18 years, and patients unwilling or unable to give informed consent patients with (clinically diagnosed) dementia and persons with insufficient German, French, Italian or English language skills)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samuel Henz, MD MPH
Organizational Affiliation
Cantonal Hospital St. Gallen, Switzerland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wolfgang Korte, MD
Organizational Affiliation
IKCH - Laboratory St. Gallen Switzerland
Official's Role
Study Director
Facility Information:
Facility Name
Cantonal Hospital St. Gallen
City
St. Gallen
ZIP/Postal Code
CH-9007
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
17350082
Citation
Good AC, Henz S. A clinical algorithm to predict the loading dose of phenprocoumon. Thromb Res. 2007;120(6):921-5. doi: 10.1016/j.thromres.2007.01.013. Epub 2007 Mar 12. No abstract available.
Results Reference
background
PubMed Identifier
23299853
Citation
Caduff Good A, Nobel D, Krahenbuhl S, Geisen C, Henz S. Randomised trial of a clinical dosing algorithm to start anticoagulation with phenprocoumon. Swiss Med Wkly. 2013 Jan 8;143:w13709. doi: 10.4414/smw.2013.13709. eCollection 2013.
Results Reference
derived

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Study to Find Out the Appropriate Initial Dose of the Anticoagulant Drug Phenprocoumon

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