This site became the new ClinicalTrials.gov on June 19th. Learn more.
Show more
ClinicalTrials.gov Menu IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more...
ClinicalTrials.gov Menu IMPORTANT: Talk with a trusted healthcare professional before volunteering for a study. Read more...
ClinicalTrials.gov Menu
Give us feedback

SPARK: Safety Study of Pradaxa in Atrial Fibrillation Patients by Regulatory Requirement of Korea

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim
ClinicalTrials.gov Identifier:
NCT01774370
First received: January 16, 2013
Last updated: June 27, 2017
Last verified: June 2017
January 16, 2013
June 27, 2017
January 14, 2013
February 17, 2017   (Final data collection date for primary outcome measure)
Occurrence of adverse events(Including unexpected adverse events, serious adverse events, drug-related adverse events, adverse events leading to discontinuation and adverse events by intensity, outcome of the event, causality) [ Time Frame: up to 26 weeks ]
Adverse events reported after intake of Pradaxa [ Time Frame: up to 26 weeks ]
Complete list of historical versions of study NCT01774370 on ClinicalTrials.gov Archive Site
  • Incidence rate of stroke [ Time Frame: up to 26 weeks ]
  • Incidence rate of systemic embolism [ Time Frame: up to 26 weeks ]
Incidence rate of stroke and systemic embolism [ Time Frame: up to 26 weeks ]
Not Provided
Not Provided
 
SPARK: Safety Study of Pradaxa in Atrial Fibrillation Patients by Regulatory Requirement of Korea
A Regulatory Requirement Non-interventional Study to Monitor the Safety and Effectiveness of Pradaxa (Dabigatran Etexilate Mesilate, 110 mg or 150 mg b.i.d.) in Korean Patients With Non-valvular Atrial Fibrillation(SPARK: Safety Study of Pradaxa in AF Patients by Regulatory Requirement of Korea)
This is a prospective, non-interventional, open-label, multi-centre study. It will provide additional safety information of Pradaxa in Korean patients with non-valvular AF in clinical settings.

Study Design:

regulatory PMS study

Observational
Observational Model: Other
Time Perspective: Prospective
Not Provided
Not Provided
Probability Sample
Korean patients with non-valvular AF
Atrial Fibrillation
Drug: Pradaxa (Dabigatran etexilate mesilate)
110 mg or 150 mg b.i.d.
Pradaxa group
Intervention: Drug: Pradaxa (Dabigatran etexilate mesilate)
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
3187
February 17, 2017
February 17, 2017   (Final data collection date for primary outcome measure)

Inclusion criteria:

  • Age >= 18 years at enrollment
  • Patients who have been started on Pradaxa in accordance with the approved label in Korea
  • Patients who have signed on the data release consent form

Exclusion criteria:

  • Patients with previous exposure to Pradaxa
  • Clinically significant bleeding
  • Increased risk of bleeding due to following diseases;

    • Recent gastrointestinal ulceration
    • Recent intracranial or intracerebral bleeding history
    • Intraspinal or intracerebral vascular abnormalities
    • Recent brain, spinal or ophthalmic surgery
    • Recent brain or spinal injury
    • Known or suspected oesophageal varices
    • Arteriovenous malformations
    • Vascular aneurysms
    • Presence of malignant neoplasms at high risk of bleeding
  • Concomitant treatment with any other anticoagulants e.g. unfractionated heparin (UFH), low molecular weight heparins (enoxaparin, dalteparin etc), heparin derivatives (fondaparinux etc), oral anticoagulants (warfarin, rivaroxaban, apixaban etc) except under the circumstances of switching therapy to or from Pradaxa or when UFH is given at doses necessary to maintain an open central venous or arterial catheter
  • Severe renal impairment (CrCl < 30mL/min)
  • Concomitant treatment with oral ketoconazole or dronedarone
  • Patients hypersensitive to dabigatran or dabigatran etexilate or to any ingredient in the formulation
  • Prosthetic heart valve replacement
  • No creatinine clearance collected within at least one year prior to enrollment
  • Current participation in other clinical trials
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Korea, Republic of
 
 
NCT01774370
1160.139
Not Provided
Not Provided
Not Provided
Not Provided
Boehringer Ingelheim
Boehringer Ingelheim
Not Provided
Study Chair: Boehringer Ingelheim Boehringer Ingelheim
Boehringer Ingelheim
June 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP