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Completed No phase listed Observational Results available

RE-COVERY DVT/PE: Global Study on Treatment Secondary Prevention of Acute Venous Thromboembolism

ClinicalTrials.gov ID: NCT02596230

Public ClinicalTrials.gov record NCT02596230. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 3:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Characterization of Patients Following Acute Venous Thromboembolism (VTE) and Safety and Effectiveness of Dabigatran Etexilate (DE) in the Treatment and Secondary Prevention of Acute Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) in Comparison to Vitamin K Antagonist (VKA) in Routine Clinical Practice - RE-COVERY DVT/PE

Study identification

NCT ID
NCT02596230
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
7,797 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 4, 2015
Primary completion
Mar 30, 2019
Completion
Mar 30, 2019
Last update posted
Apr 28, 2020

2015 – 2019

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Cardiovascular Innovation and Research Center Long Beach California 90813
Health and Life Research Institute, LLC Miami Florida 33155
Med-Care Research Miami Florida 33165
Pines Care Research Center Pembroke Pines Florida 33026
Tampa General Hospital Tampa Florida 33606
Ellipsis Group Atlanta Georgia 30342
Wellstar Cardiovascular Medicine Marietta Georgia 30060
Fox Valley Clinical Research Center, LLC Aurora Illinois 60504
Johns Hopkins University Baltimore Maryland 21205
Genesys Regional Medical Center Grand Blanc Michigan 48439
University Of Mississippi Medical Center Jackson Mississippi 39216
Vidant Multispecialty Clnc Kinston Kinston North Carolina 28501
Sanford Cardiology Sanford North Carolina 27330
Lycoming Internal Medicine, Inc Jersey Shore Pennsylvania 17740
Research Associates of Jackson Jackson Tennessee 38301
The University Of Texas at Houston Houston Texas 77030
Cardiology Center of Houston, PA Katy Texas 77450
Cardio Voyage McKinney Texas 75071
Waukesha Heart Institute Waukesha Wisconsin 53188

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 203 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02596230, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 28, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02596230 live on ClinicalTrials.gov.

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