Evaluate Advanced Pneumatic Compression Device With Revised Compression Programming for Lymphedema Treatment

Part of paid clinical trials in Houston, Texas.

Sponsor
Tactile Medical
Study ID
NCT07613931
Phase
EARLY_PHASE1
Status
Recruiting

Conditions

  • Lower Extremity Lymphedema

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Advanced pneumatic compression device (APCD) — DEVICE
    Single APCD treatment session at visit 1
  • Advanced pneumatic compression device (APCD) with revised compression programming — DEVICE
    APCD with revised compression programming will be single treatment session at visit 2
  • Indocyanine Green (IC-Green) — DRUG
    Indocyanine Green dye will be used to assess primary endpoint

Study Details

The goal of this pilot study is to learn if a revised method of compression improves lymphatic function compared to the current method of compression. The main questions: • Does the revised method of compression improve lymph movement and lymphatic propulsion?

Key Dates

First listed
May 29, 2026
Start date
Jul 31, 2026
Status verified
Jul 2026
Primary completion
Sep 30, 2026
Completion
Sep 30, 2026

Study Design

Enrollment
5 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY

Arms

  • Experimental: Treatment group

Primary Outcome Measure

Lymphatic anatomy [ Time Frame: Before and after 60-minute treatment in clinic with APCD ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
UTHealth Houston (The University of Texas Health Science Center at Houston)HoustonTexas77030
John Rasmussen, PhD
713-500-3393

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