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Frankfurt Thrombophilia Registry

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00683397
First Posted: May 23, 2008
Last Update Posted: April 19, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Prof. Dr. med. E. Lindhoff-Last, Cardioangiologisches Centrum Bethanien
  Purpose
Consecutive patients with acute or previous venous thromboembolism are enrolled in this registry. Using a standardized questionnaire, clinical data detailing venous thromboembolism and contributing VTE risk factors are recorded. Results of technical and laboratory investigations including screening for thrombophilic disorders were additionally entered into the database.

Condition Intervention
Venous Thromboembolism Other: Blood sampling

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Frankfurt Thrombophilia Registry - Evaluation of Patients With Venous Thromboembolism

Resource links provided by NLM:


Further study details as provided by Prof. Dr. med. E. Lindhoff-Last, Cardioangiologisches Centrum Bethanien:

Biospecimen Retention:   Samples With DNA
whole blood, serum

Enrollment: 2000
Study Start Date: May 2008
Study Completion Date: December 2014
Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
A
Patients with acute or previous venous thromboembolism >18 years of age
Other: Blood sampling
Screening of thrombophilia

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
consecutive patients with acute or previous VTE >18 years of age
Criteria

Inclusion Criteria:

  • Acute or previous VTE

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00683397


Locations
Germany
Cardioangiologisches Centrum Bethanien
Frankfurt/Main, Hessen, Germany, 60389
Sponsors and Collaborators
Cardioangiologisches Centrum Bethanien
Investigators
Principal Investigator: Edelgard Lindhoff-Last, Professor Cardioangiologisches Zentrum Bethanien
  More Information

Publications:

Responsible Party: Prof. Dr. med. E. Lindhoff-Last, M.D., Cardioangiologisches Centrum Bethanien
ClinicalTrials.gov Identifier: NCT00683397     History of Changes
Other Study ID Numbers: MAISTHRO Study 93/08
First Submitted: May 21, 2008
First Posted: May 23, 2008
Last Update Posted: April 19, 2017
Last Verified: April 2017

Keywords provided by Prof. Dr. med. E. Lindhoff-Last, Cardioangiologisches Centrum Bethanien:
assess
prevalence
thrombophilia
common
VTE
risk factors
patients

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