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Treatment Trial for Post-Thrombotic Syndrome

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University of Vermont

Status

Completed

Conditions

Post Thrombotic Syndrome

Treatments

Other: complex lymphedema therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT00633971
CHRMS 08-065

Details and patient eligibility

About

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.

Full 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.

Enrollment

31 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

31 participants in 2 patient groups

A
Experimental group
Description:
Complex lymphedema therapy (which includes compression stocking use)
Treatment:
Other: complex lymphedema therapy
B
Other group
Description:
Standard of care (compression stocking use at 30-40 mm Hg)
Treatment:
Other: complex lymphedema therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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