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) — DEVICESingle APCD treatment session at visit 1
- Advanced pneumatic compression device (APCD) with revised compression programming — DEVICEAPCD with revised compression programming will be single treatment session at visit 2
- Indocyanine Green (IC-Green) — DRUGIndocyanine 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
- Senior Vice President Marketing and Market Access1.833.382.2845
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UTHealth Houston (The University of Texas Health Science Center at Houston) | Houston | Texas | 77030 |