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Completed Phase 2 Interventional Results available

PETRO Stroke Prevention in Patients With AF by Treatment With Dabigatran, With and Without Aspirin, Compared to Warfarin

ClinicalTrials.gov ID: NCT01227629

Public ClinicalTrials.gov record NCT01227629. 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 Jun 25, 2026, 10:29 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

Dose Exploration in Patients With Atrial Fibrillation

Study identification

NCT ID
NCT01227629
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
502 participants

Conditions and interventions

Interventions

  • dabigatran with ASA Drug
  • warfarin Drug
  • dabigatran without ASA Drug

Drug

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
Aug 31, 2003
Primary completion
Oct 31, 2004
Completion
Not listed
Last update posted
May 4, 2014

Started 2003

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
1160.20.10010 Fayetteville Arkansas
1160.20.10003 La Mesa Cardiac La Mesa California
1160.20.10006 The Ford Research Institute, PA Pensacola Florida
1160.20.10004 Port Charlotte Florida
1160.20.10002 St. Petersburg Florida
1160.20.10015 Baltimore Maryland
1160.20.10008 Westminister Maryland
1160.20.10012 Pittsfield Massachusetts
1160.20.10007 Troy Michigan
1160.20.10014 Hawthorne New York
1160.20.10013 New Hyde Park New York
1160.20.10009 North Durham North Carolina
1160.20.10001 Philadelphia Pennsylvania
1160.20.10005 Germantown Tennessee

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01227629, 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 May 4, 2014 · Synced Jun 25, 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 protocol, eligibility criteria, and contact information for NCT01227629 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →