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| 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 |
| Estimated Enrollment: | 3505 |
| Estimated Study Completion Date: | July 2006 |
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 |
Inclusion criteria (selected):
Exclusion criteria (selected):
Contacts and Locations
Hide Study 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 | |
| Study Chair: | Boehringer Ingelheim Study Coordinator | Boehringer Ingelheim BV/Alkmaar |
More Information
| 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 |
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Embolism and Thrombosis Vascular Diseases Cardiovascular Diseases Thrombosis Thromboembolism |