Recruiting

Observational Study

Sponsor:

Heart and Vascular Outcomes Research Institute

Code:

NCT02113475

Conditions

Deep Venous Thrombosis

Post Thrombotic Syndrome

Eligibility Criteria

Sex: All

Age: 16 - 70+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

Deep Venous Thrombosis affects more than 350,000 individuals each year in the U.S.The Registry will track patient outcome and quality of life over 60 months for treatment with anticoagulation and elastic compression stockings and catheter-directed thrombolysis (CDT) in accordance with current treatment guidelines .

Conditions

Deep Venous Thrombosis

Post Thrombotic Syndrome

Study ID

NCT02113475

Start date

Apr, 2014

Status verified date

Mar, 2015

Completion date

Jan, 2021

Anticipated

Primary completion date

Mar, 2020

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 16 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

•Data obtained in line with good clinical practice, applicable laws and regulation

Exclusion Criteria:

-

Study Design

Enrollment

1800 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • Quality of Life, [ Time Frame: 60 months ]

Central Contacts and Locations

Central contacts

Uchenna N Onyeachom

978-927-7800uonyeachom@hvori.org

Locations

Heart & Vascular Outcomes Research Institute

Recruiting

Beverly, Massachusetts, United States, 01915

More Information

Sponsor

Heart and Vascular Outcomes Research Institute

Last update posted

Mar 19, 2015

Last verified

Mar, 2015

Keywords

  • CDT
  • PCDT
  • DVT
  • PTS
  • Quality of Life

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Heart and Vascular Outcomes Research Institute on 2015-03-19.