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Dabigatran Etexilate in Extended VTE Prevention After Hip Replacement Surgery
This study has been completed.
First Received: September 12, 2005   Last Updated: September 29, 2009   History of Changes
Sponsor: Boehringer Ingelheim Pharmaceuticals
Information provided by: Boehringer Ingelheim Pharmaceuticals
ClinicalTrials.gov Identifier: NCT00168818
  Purpose

The objective of this study is to determine the comparative efficacy and safety of two oral regimens of dabigatran etexilate, compared to a standard subcutaneous regimen of enoxaparin, in prevention o f venous thromboembolism (e.g. deep vein thrombosis of the leg) in patients with primary elective to tal hip replacement surgery.


Condition Intervention Phase
Thromboembolism
Arthroplasty, Replacement, Hip
Drug: "Dabigatran etexilate (oral, 150 mg once daily)"
Drug: "Enoxaparin (subcutaneous, 40 mg once daily)"
Drug: "Dabigatran etexilate (oral, 220 mg once daily)"
Phase III

Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study
Official Title: A Phase III Randomised, Parallel Group, Double-blind, Active Controlled Study to Investigate the Efficacy and Safety of Two Different Dose Regimens of Orally Administered Dabigatran Etexilate Capsules [150 or 220 mg Once Daily Starting With Half Dose (i.e. 75 or 110 mg) on the Day of Surgery] Compar

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Further study details as provided by Boehringer Ingelheim Pharmaceuticals:

Primary Outcome Measures:
  • Total venous thromboembolic events (VTE) and all cause mortality during the treatment period. Total VTE is defined as the composite incidence of proximal and distal deep venous thrombosis (DVT), symptomatic DVT and pulmonary embolism (PE).

Secondary Outcome Measures:
  • Efficacy: Major VTE (proximal DVT and PE) and VTE related mortality proximal DVT total DVT symptomatic DVT PE death Safety: Bleeds blood loss + transfusion adverse events (AE) discontinuation due to AE laboratory physical exam.

Estimated Enrollment: 3505
Estimated Study Completion Date: July 2006
Detailed Description:

This is a phase III randomised, parallel group, double-blind, active controlled (double dummy) study to investigate the efficacy and safety of two different dose regimens of orally administered dabiga tran etexilate capsules [150 or 220 mg once daily starting with half dose (i.e. 75 or 110 mg) on the day of surgery] compared to subcutaneous enoxaparin 40 mg once daily for 28-35 days, in prevention of venous thromboembolism in patients with primary elective total hip replacement surgery.

Study Hypothesis:

This trial aims to demonstrate therapeutic equivalence (non-inferiority) of dabi gatran compared with enoxaparin by showing that the rate of total venous thrombo embolic events (VTE) plus all-cause mortality in dabigatran treatment does not e xceed the VTE rate after enoxaparin treatment by more than 7.7%. The correspondi ng null hypotheses of interest are that the difference in rates of total VTE plu s all-cause mortality in dabigatran treatment versus enoxaparin is greater than 7.7%.

Comparison(s):

For the primary comparison the rates of total venous thromboembolic events (VTE) and all cause mortality during the treatment period will be compared. Total VTE is defined as the composite incidence of proximal and distal deep venous thromb osis (DVT), symptomatic DVT and pulmonary embolism (PE).

  Eligibility

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

Inclusion criteria (selected):

  • Patients (18 years or older) scheduled to undergo a primary, unilateral, elect ive total hip replacement
  • Written Informed Consent

Exclusion criteria (selected):

  • Patients with an excessive risk of bleeding, for example because of history o f bleeding diathesis major surgery or trauma within the last 3 months history of haemorrhagic stroke or any of the following intracranial pathologies: bleedin g, neoplasm, AV malformation or aneurysm clinically relevant bleeding or gastri c / duodenal ulcer within the last 6 months treatment with anticoagulants withi n 7 days prior to joint replacement surgery or anticipated need during the study treatment period thrombocytopenia.
  • Active malignant disease or current cytostatic treatment
  • Known severe renal insufficiency
  • Liver disease expected to have any potential impact on survival, or elevated A ST or ALT > 2x upper limit of normal
  • Recent unstable cardiovascular disease or history of myocardial infarction wit hin the last 3 months
  • Pre-menopausal women who are pregnant or nursing, or are of child-bearing pote ntial and are not practising or do not plan to continue practising acceptable me thods of birth control
  • Allergy to radio opaque contrast media or iodine, heparins (incl. heparin indu ced thrombocytopenia) or dabigatran
  • Contraindications to enoxaparin
  • Participation in a clinical trial during the last 30 days
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00168818

  Hide Study Locations
Locations
Australia, Australian Capital Territory
Canberra Hospital
Garren, Australian Capital Territory, Australia, 2605
Australia, New South Wales
St George Public Hospital
KOGARAH, New South Wales, Australia, 2217
Suite 13 level 4
Lismore, New South Wales, Australia, 2480
Australia, South Australia
Flinders Medical Centre
Bedford Park, South Australia, Australia, 5042
Australia, Victoria
Boehringer Ingelheim Investigational Site
Clayton, Victoria, Australia, 3168
ECRU
Box Hill, Victoria, Australia, 3128
Maroondah Hospital
Ringwood East, Victoria, Australia, 3135
Emeritus Research
MALVERN, Victoria, Australia, 3144
Boehringer Ingelheim Investigational Site
Windsor, Victoria, Australia, 3181
Australia, Western Australia
Haemophillia & Thrombosis Service
Perth, Western Australia, Australia, 6847
Austria
Boehringer Ingelheim Investigational Site
Wr. Neustadt, Austria, 2700
Boehringer Ingelheim Investigational Site
Linz, Austria, 4010
Boehringer Ingelheim Investigational Site
Wels, Austria, 4600
Boehringer Ingelheim Investigational Site
Wien, Austria, 1130
Belgium
UVC Brugmann
Brussels, Belgium, 1020
UZ Gent
Gent, Belgium, 9000
UZ Gasthuisberg
Leuven, Belgium, 3000
Virga Jesseziekenhuis
Hasselt, Belgium, 3500
Campus Sint-Lucas
Gent, Belgium, 9000
Ziekenhuis Oost-Limburg
Lanaken, Belgium, 3620
AZ Sint Elisabeth
Herentals, Belgium, 2200
Czech Republic
Boehringer Ingelheim Investigational Site
Pradubice, Czech Republic, 530 03
Boehringer Ingelheim Investigational Site
Kladno, Czech Republic, 272 59
Boehringer Ingelheim Investigational Site
Ostrava, Czech Republic, 708 52
Boehringer Ingelheim Investigational Site
Brno-Bohunice, Czech Republic, 625 00
Boehringer Ingelheim Investigational Site
Prague 8, Czech Republic, 180 81
Boehringer Ingelheim Investigational Site
Kolin, Czech Republic, 280 00
Boehringer Ingelheim Investigational Site
Plzen, Czech Republic, 304 60
Boehringer Ingelheim Investigational Site
Jihlava, Czech Republic, 586 01
Boehringer Ingelheim Investigational Site
Havlickuv Brod, Czech Republic, 580 01
Boehringer Ingelheim Investigational Site
Chomutov, Czech Republic, 430 01
Denmark
Boehringer Ingelheim Investigational Site
H?rsholm, Denmark, DK-2970
Boehringer Ingelheim Investigational Site
Silkeborg, Denmark, 8600
Boehringer Ingelheim Investigational Site
K?benhavn NV, Denmark, 2400
Boehringer Ingelheim Investigational Site
K?benhavn S, Denmark, 2400
Boehringer Ingelheim Investigational Site
Hellerup, Denmark, DK-2900
Finland
Boehringer Ingelheim Investigational Site
Oulu, Finland, FI-90029 OYS
Boehringer Ingelheim Investigational Site
Jyvaskyla, Finland, FI-40620
Boehringer Ingelheim Investigational Site
Tampere, Finland, FI-33101
Boehringer Ingelheim Investigational Site
Helsinki, Finland, FI-00280
Boehringer Ingelheim Investigational Site
Seinajoki, Finland, FI-60220
France
Boehringer Ingelheim Investigational Site
Soyaux, France, 16800
Boehringer Ingelheim Investigational Site
Roubaix cedex, France, 59056
Boehringer Ingelheim Investigational Site
Amiens cedex 1, France, 80054
Boehringer Ingelheim Investigational Site
Strasbourg, France, 67000
Germany
Kreiskrankenhaus
Rheinfelden, Germany, 79618
Klinikum Garmisch-Partenkirchen
Garmisch-Partenkirchen, Germany, 82467
Aukammklinik
Wiesbaden, Germany, 65191
Orthopadische Universitatsklinik
Frankfurt, Germany, 60528
Hellmuth-Ulrici-Kliniken
Sommerfeld, Germany, 16766
Caritaskrankenhaus
Bad Mergentheim, Germany, 97980
Johannes Gutenberg-Universitat Mainz
Mainz, Germany, 55101
F.-A.-Universitat Erlangen-Nurnberg
Erlangen, Germany, 91054
Orthopadische Klinik Markgroningen gGmbH
Markgroningen, Germany, 71706
St. Bernhard-Hospital
Kamp-Lintfort, Germany, 47475
Orthopadische Klinik Lindenlohe
Schwandorf, Germany, 92421
Hungary
Boehringer Ingelheim Investigational Site
Gyula, Hungary, 5700
Boehringer Ingelheim Investigational Site
Szeged, Hungary, 6720
Boehringer Ingelheim Investigational Site
Budapest, Hungary, 1076
Boehringer Ingelheim Investigational Site
Kecskemet, Hungary, 6000
Boehringer Ingelheim Investigational Site
Szekesfehervar, Hungary, 8001
Boehringer Ingelheim Investigational Site
Budapest, Hungary, 1125
Boehringer Ingelheim Investigational Site
Bekescsaba, Hungary, 5600
Italy
Boehringer Ingelheim Investigational Site
PAVIA, Italy, 27100
Boehringer Ingelheim Investigational Site
Milano, Italy, 20132
Boehringer Ingelheim Investigational Site
BOLOGNA, Italy, 40136
Boehringer Ingelheim Investigational Site
Bergamo, Italy, 24128
Netherlands
Boehringer Ingelheim Investigational Site
Heemstede, Netherlands, 2102 CW
Boehringer Ingelheim Investigational Site
Amsterdam, Netherlands, 1105 AZ
Boehringer Ingelheim Investigational Site
Sittard, Netherlands, 6131 BK
Boehringer Ingelheim Investigational Site
Nijmegen, Netherlands, 6522 JV
Boehringer Ingelheim Investigational Site
Hilversum, Netherlands, 1243 XZ
Boehringer Ingelheim Investigational Site
Helmond, Netherlands, 5707 HA
Norway
Boehringer Ingelheim Investigational Site
BOD?, Norway, N-8005
Boehringer Ingelheim Investigational Site
SKIEN, Norway, N-3710
Boehringer Ingelheim Investigational Site
?LESUND, Norway, N-6017
Boehringer Ingelheim Investigational Site
B?RUM POSTTERMINAL, Norway, N-1306
Boehringer Ingelheim Investigational Site
ELVERUM, Norway, N-2418
Boehringer Ingelheim Investigational Site
B?RUM POSTTERMINAL, Norway, N-1306
Poland
Boehringer Ingelheim Investigational Site
Piekary Slaskie, Poland, 42-640
Boehringer Ingelheim Investigational Site
Warsaw, Poland, 01-809
Boehringer Ingelheim Investigational Site
Warsaw, Poland, 00-909
Boehringer Ingelheim Investigational Site
Kielce, Poland, 25-736
Boehringer Ingelheim Investigational Site
Krakow, Poland, 30-224
Boehringer Ingelheim Investigational Site
Krakow, Poland, 31-826
Boehringer Ingelheim Investigational Site
Warsaw, Poland, 02-637
Boehringer Ingelheim Investigational Site
Bialystok, Poland, 15-276
Boehringer Ingelheim Investigational Site
Mielec, Poland, 39-300
Boehringer Ingelheim Investigational Site
Rzeszow, Poland, 35-301
Boehringer Ingelheim Investigational Site
Lodz, Poland, 95-513
South Africa
Boehringer Ingelheim Investigational Site
Randburg, South Africa, 2158
Boehringer Ingelheim Investigational Site
Sandton, South Africa, 2057
Boehringer Ingelheim Investigational Site
Bryanston, South Africa, 2060
Boehringer Ingelheim Investigational Site
Johannesburg, South Africa, 2192
Spain
Boehringer Ingelheim Investigational Site
Madrid, Spain, 28040
Boehringer Ingelheim Investigational Site
Madrid, Spain, 28046
Boehringer Ingelheim Investigational Site
Barcelona, Spain, 08036
Boehringer Ingelheim Investigational Site
Hospitalet (Barcelona), Spain, 08907
Boehringer Ingelheim Investigational Site
Alcorcon (Madrid), Spain, 28922
Boehringer Ingelheim Investigational Site
Madrid, Spain, 28034
Boehringer Ingelheim Investigational Site
Mostoles (Madrid), Spain, 28935
Boehringer Ingelheim Investigational Site
Jaen, Spain, 23009
Boehringer Ingelheim Investigational Site
Valencia, Spain, 46010
Boehringer Ingelheim Investigational Site
Barcelona, Spain, 08035
Sweden
Boehringer Ingelheim Investigational Site
Goteborg, Sweden, 416 85
Boehringer Ingelheim Investigational Site
Falkoping, Sweden, 521 85
Boehringer Ingelheim Investigational Site
Kungalv, Sweden, 442 83
Boehringer Ingelheim Investigational Site
Stockholm, Sweden, 118 83
Boehringer Ingelheim Investigational Site
Linkoping, Sweden, 591 85
Boehringer Ingelheim Investigational Site
Kalmar, Sweden, 391 85
Boehringer Ingelheim Investigational Site
Halmstad, Sweden, 301 85
Boehringer Ingelheim Investigational Site
Lidkoping, Sweden, 531 85
Boehringer Ingelheim Investigational Site
Varberg, Sweden, 432 81
Boehringer Ingelheim Investigational Site
Molndal, Sweden, 431 80
Sponsors and Collaborators
Boehringer Ingelheim Pharmaceuticals
Investigators
Study Chair: Boehringer Ingelheim Study Coordinator Boehringer Ingelheim BV/Alkmaar
  More Information

Additional Information:
No publications provided by Boehringer Ingelheim Pharmaceuticals

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Study ID Numbers: 1160.48
Study First Received: September 12, 2005
Last Updated: September 29, 2009
ClinicalTrials.gov Identifier: NCT00168818     History of Changes
Health Authority: Sweden: MPA;   Finland: Finnish Medicines Agency;   Denmark: Danish Medicines Agency;   Norway: Norwegian Medicines Agency;   Netherlands: The Central Committee on Research Involving Human Subjects (CCMO);   Austria: Federal Ministry of Health and Women and Generations;   Belgium: Directorate-General Public Health Protection Medicinal Products;   France: Agence Francaise de Securite Sanitaire des Produits de Sante;   Germany: Bundesamt fuer Strahlenschutz;   South Africa: Medicines Control Council;   Spain: Agencia Espa?ola de Medicamentos y Productos Santarios;   Austria: SUKL;   Austria: CEBK;   Australia: Therapeutic Goods Administration;   Italy: Comitato di Bioetica IRCCS Policlinico San Matteo

Additional relevant MeSH terms:
Embolism and Thrombosis
Vascular Diseases
Cardiovascular Diseases
Thrombosis
Thromboembolism

ClinicalTrials.gov processed this record on November 27, 2009