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Completed Phase 2 Interventional Results available

A Randomized, Open-Label, Parallel-Group, Multi-Center Study for the Evaluation of Efficacy and Safety of Edoxaban Monotherapy Versus Low Molecular Weight (LMW) Heparin/Warfarin in Subjects With Symptomatic Deep-Vein Thrombosis

ClinicalTrials.gov ID: NCT01662908

Public ClinicalTrials.gov record NCT01662908. 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 Sep 1, 2026, 1:41 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

A Randomized, Open-Label, Parallel-Group, Multi-Center Study for the Evaluation of Efficacy and Safety of Edoxaban Monotherapy Versus (LMW) Heparin/Warfarin in Subjects With Symptomatic Deep-Vein Thrombosis - Edoxaban Thrombus Reduction Imaging Study

Brief summary

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

Assess the relative change in thrombus volume as determined by two assessments (Baseline and Day 14-21) with magnetic resonance venography (MRV) in subjects with deep-vein thrombosis (DVT) treated with either an edoxaban monotherapy regimen or a low molecular weight (LMW) heparin/warfarin regimen.

Study identification

NCT ID
NCT01662908
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Daiichi Sankyo
Industry
Enrollment
85 participants

Conditions and interventions

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
Jul 31, 2012
Primary completion
Dec 31, 2013
Completion
Feb 28, 2014
Last update posted
Feb 25, 2019

2012 – 2014

United States locations

U.S. sites
29
U.S. states
17
U.S. cities
29
Facility City State ZIP Site status
Not listed Dothan Alabama
Not listed Montgomery Alabama
Not listed Sacramento California
Not listed Atlantis Florida
Not listed Clearwater Florida
Not listed Fort Myers Florida
Not listed Jacksonville Florida
Not listed Sarasota Florida
Not listed Tampa Florida
Not listed Jonesboro Georgia
Not listed Lafayette Indiana
Not listed Paducah Kentucky
Not listed Covington Louisiana
Not listed Annapolis Maryland
Not listed Baltimore Maryland
Not listed Randallstown Maryland
Not listed Butte Montana
Not listed Grand Island Nebraska
Not listed Rochester New York
Not listed Durham North Carolina
Not listed Greensboro North Carolina
Not listed Wilmington North Carolina
Not listed Maumee Ohio
Not listed Camp Hill Pennsylvania
Not listed Ephrata Pennsylvania
Not listed Sellersville Pennsylvania
Not listed Rapid City South Dakota
Not listed Fredericksburg Virginia
Not listed Tacoma Washington

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01662908, 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 Feb 25, 2019 · Synced Sep 1, 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 NCT01662908 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →