NCT05507346View on ClinicalTrials.gov

A Clinical Study to Evaluate the Effectiveness of a Novel Portable Non-Pneumatic Active Compression Device vs. an Advanced Pneumatic Compression Device for Treating Lower Extremity Lymphedema

NACompletedINTERVENTIONAL
Enrollment

121

Participants

Timeline

Start Date

September 6, 2022

Primary Completion Date

January 9, 2024

Study Completion Date

January 9, 2024

Conditions
LymphedemaLymphedema of LegChronic Venous InsufficiencyVenous InsufficiencyLymphedema, Lower Limb
Interventions
DEVICE

Cross over Device (PCD or Dayspring - alternate to first group)

Cross over after three month of use and a month of washout period

Trial Locations (1)

94607

Stanley G Rockson, Oakland

Sponsors

Lead Sponsor

Koya Medical, Inc.
All Listed Sponsors
lead

Koya Medical, Inc.

INDUSTRY