Quality of Life Changes on Lower Extremity Lymphedema Patients Using an Advanced Pneumatic Compression Device (PCD)

NCT02661646 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 249

Last updated 2023-04-03

No results posted yet for this study

Summary

Assessment of quality of life and symptoms changes in primary or secondary, unilateral or bilateral lower extremity lymphedema patients using an advanced pneumatic compression system.

Conditions

  • Lymphedema

Interventions

DEVICE

Advanced Pneumatic Compression Device

Advanced Pneumatic Compression Device

Sponsors & Collaborators

  • Tactile Medical

    lead INDUSTRY

Principal Investigators

  • Thomas Maldonado, MD · NYU

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-12-31
Primary Completion
2023-02-01
Completion
2023-02-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02661646 on ClinicalTrials.gov