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Completed No phase listed Observational Results available

Management of Gastrointestinal and Urogenital (GI/GU) Bleedings in Atrial Fibrillation Patients Using Pradaxa

ClinicalTrials.gov ID: NCT02022020

Public ClinicalTrials.gov record NCT02022020. 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 Oct 27, 2026, 2:08 AM EDT

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

Official title

An Observational Study Assessing the Management of Gastrointestinal and Urogenital Bleeding Events in Patients With Atrial Fibrillation Treated With Dabigatran Etexilate

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is being conducted to collect data on the management of gastrointestinal and urogenital bleeding events occurring in patients with atrial fibrillation taking dabigatran etexilate.

Study identification

NCT ID
NCT02022020
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
220 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
Jan 2014 (Type not available)
Primary completion
Oct 2015 (Actual)
Completion
Oct 2015 (Actual)
Last update posted
Jan 31, 2017

2014 – 2015

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Boehringer Ingelheim Investigational Site Aurora Colorado — —
Boehringer Ingelheim Investigational Site New Britain Connecticut — —
Boehringer Ingelheim Investigational Site Orlando Florida — —
Boehringer Ingelheim Investigational Site Tampa Florida — —
Boehringer Ingelheim Investigational Site New Orleans Louisiana — —
Boehringer Ingelheim Investigational Site Springfield Massachusetts — —
Boehringer Ingelheim Investigational Site Chesterfield Missouri — —
Boehringer Ingelheim Investigational Site St Louis Missouri — —
Boehringer Ingelheim Investigational Site Hackensack New Jersey — —
Boehringer Ingelheim Investigational Site New York New York — —
Boehringer Ingelheim Investigational Site Staten Island New York — —
Boehringer Ingelheim Investigational Site Philedelphia Pennsylvania — —
Boehringer Ingelheim Investigational Site Nashville Tennessee — —
Boehringer Ingelheim Investigational Site Charlottesville Virginia — —
Boehringer Ingelheim Investigational Site Norfolk Virginia — —
Boehringer Ingelheim Investigational Site Roanoke Virginia — —

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02022020, 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 Jan 31, 2017 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02022020 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →