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Treatment Trial for Post-Thrombotic Syndrome

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00633971
Enrollment
31
Registered
2008-03-12
Start date
2008-03-31
Completion date
2011-09-30
Last updated
2020-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Thrombotic Syndrome

Keywords

Post thrombotic syndrome, Thrombosis, Deep vein thrombosis, Venous thrombosis, Edema, stasis ulcers

Brief summary

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.

Detailed description

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.

Interventions

OTHERcomplex lymphedema therapy

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

Sponsors

University of Vermont
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
To determine if complex lymphedema therapy improves the quality of life in patients with post-thrombotic syndrome1 and 3 months
To determine if complex lymphedema therapy reduces disease severity in patients with post thrombotic syndrome1 and 3 months

Secondary

MeasureTime frame
To assess side effects of lymphedema therapy when administered to patients with PTS1 and 3 months
To determine if selected biomarkers correlate with disease severity and response to lymphedema therapy in patients with post thrombotic syndrome1 and 3 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026