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Completed

NCT Number: NCT00633971

Treatment Trial for Post-Thrombotic Syndrome

The purpose of this study is to determine if complex lymphedema therapy is effective in decreasing disease severity and improving quality of life in patients with post thrombotic syndrome.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fletcher Allen Health Care; Department of Hematology/Oncology

Burlington, Vermont, 05401, United States

About this study

Post thrombotic syndrome (PTS) has a spectrum of disease manifestations ranging from minor skin discoloration to severe skin changes and venous ulcerations. Pain is often a prominent symptoms and PTS impairs patient quality of life. Prevention of PTS using compression stockings has been emphasized. There is a paucity of validated, effective treatments for PTS once the condition develops.

While the pathophysiology of PTS is incompletely understood, chronic venous hypertension and insufficiency may increase the workload of the lymphatic system and result in over-capacitance with secondary damage and eventual lymphatic insufficiency. In selected patients with PTS, we have noted a symptomatic improvement in patients who receive lymphedema therapy to the limb.

Complex lymphedema therapy (CLT) is a noninvasive treatment that includes four key components: meticulous skin care, manual lymph drainage, compression therapy, exercises and patient education for home management and continuation of the treatment. These techniques are designed to enhance lymph flow through intact cutaneous lymphatics and reduce swelling and restore function in the affected limb.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18 years.
  • Diagnosis of post thrombotic syndrome.
  • Median life expectancy of greater than 2 years.
  • Previous history of lower extremity deep venous thrombosis.

Exclusion criteria

  • Acute venous thrombosis of the lower extremity within the last 180 days.
  • Unable to participate in lymphedema therapy due to monetary, physical or transportation limitations.
  • Uncontrolled illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • Pregnant women and women in their first post-partum month.

Treatment and study plan

complex lymphedema therapy

Other

Patients with established post thrombotic syndrome will be randomized to either compression stocking use or complex lymphedema therapy.

Primary outcomes

  1. To determine if complex lymphedema therapy improves the quality of life in patients with post-thrombotic syndrome

    Time frame: 1 and 3 months

  2. To determine if complex lymphedema therapy reduces disease severity in patients with post thrombotic syndrome

    Time frame: 1 and 3 months

Secondary outcomes

  1. To assess side effects of lymphedema therapy when administered to patients with PTS

    Time frame: 1 and 3 months

  2. To determine if selected biomarkers correlate with disease severity and response to lymphedema therapy in patients with post thrombotic syndrome

    Time frame: 1 and 3 months

Sponsors and collaborators

Lead sponsor

University of Vermont

Other

Registry information

Official study title

A Randomized Trial to Determine the Impact of Lymphedema Therapy on Quality of Life and Disease Severity in Patients With Post-Thrombotic Syndrome

Important dates

Study start
2008
Primary completion
2010
Study completion
2011
First posted
Mar 12, 2008
Registry last updated
Sep 17, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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