Actively Recruiting
Evaluating the Hemodynamic Performance of the VenAir Sequential Compression System
Led by Wellell Inc. Taiwan · Updated on 2026-01-06
105
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn an Intermittent Pneumatic Compression Device (IPCD), VenAir, effectiveness in healthy adults. The main questions this research aims to answer are: 1. The hemodynamic performance of VenAir paired with the thigh garments, calf garments, and foot garments is not inferior to that of SCD700 paired with the corresponding garments. 2. The hemodynamic performance of VenAir paired with the thigh garments, calf garments, and foot garments is not inferior to that of SCD700 paired with the thigh garment. Researchers will compare VenAir and the SCD700 to see if the hemodynamic performance of VenAir is as well as or not worse than the SCD700. Participants will lie down and rest for approximately 30 minutes to stabilize their heart rate. The researcher will then use ultrasound to measure the participant's blood flow while they wear different leg garments (one at a time) and also when no garment is worn.
CONDITIONS
Official Title
Evaluating the Hemodynamic Performance of the VenAir Sequential Compression System
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy adults
- Aged 20-64 years
- Leg circumference within the size range of the SCD700 and VenAir garments
You will not qualify if you...
- Cardiovascular-related diseases (mild atherosclerosis, other ischemic vascular diseases, congestive heart failure, etc.)
- Previous suspicion of deep vein thrombosis, pulmonary embolism, or phlebitis
- History of stroke
- History of varicose vein surgery
- Hypertension
- Diabetes
- Dermatitis, gangrene, or severe wounds
- Massive edema of legs
- Pregnancy
- Pulmonary edema
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Wellell Inc.
New Taipei City, Taiwan, 236044
Actively Recruiting
Research Team
C
Cheng Yung Chang
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
OTHER
Number of Arms
2
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