RECRUITINGOBSERVATIONAL
Clinical Application of Wearable Ultrasound Sensors
Clinical Application on the R&D Purpose of Wearable Ultrasound Sensors:A Single-Center Prospective Study
About This Trial
This study aims to develop and evaluate a wearable ultrasound imaging sensor for the early diagnosis and real-time monitoring of various diseases, such as cardiovascular conditions and structural abnormalities of superficial organs. With advancements in medical technology, wearable devices have attracted increasing attention for their portability and real-time capabilities.
Who May Be Eligible (Plain English)
Who May Qualify:
- Age ≥ 18 yrs and able to consent
- Relevant diagnosis for study arm (heart failure, lower-limb DVT, or ICU monitoring)
- Adequate acoustic window and intact skin at sensor site
Arm-specific:
- Heart-failure arm: Clinically stable HFrEF or HFpEF on standard therapy
- DVT arm: Imaging-confirmed lower-limb DVT, anticoagulated or scheduled for intervention
- ICU arm: ICU/post-op patient requiring continuous bedside ultrasound
Who Should NOT Join This Trial:
- Poor acoustic window preventing interpretable images
- Local skin infection, open wound, or implant/hardware blocking sensor
- Inability to cooperate with monitoring
Arm-specific:
- Heart-failure arm: Acute MI or uncontrolled arrhythmia in past 3 months
- DVT arm: Active bleeding or severe coagulopathy
- ICU arm: Unstable multi-organ failure precluding safe monitoring
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Age ≥ 18 yrs and able to consent
* Relevant diagnosis for study arm (heart failure, lower-limb DVT, or ICU monitoring)
* Adequate acoustic window and intact skin at sensor site
Arm-specific:
* Heart-failure arm: Clinically stable HFrEF or HFpEF on standard therapy
* DVT arm: Imaging-confirmed lower-limb DVT, anticoagulated or scheduled for intervention
* ICU arm: ICU/post-op patient requiring continuous bedside ultrasound
Exclusion Criteria:
* Poor acoustic window preventing interpretable images
* Local skin infection, open wound, or implant/hardware blocking sensor
* Inability to cooperate with monitoring
Arm-specific:
* Heart-failure arm: Acute MI or uncontrolled arrhythmia in past 3 months
* DVT arm: Active bleeding or severe coagulopathy
* ICU arm: Unstable multi-organ failure precluding safe monitoring
Treatments Being Tested
OTHER
This study is designed to assess the non-inferiority of a novel ultrasound imaging technique, rather than to evaluate a therapeutic intervention.
This study is designed to assess the non-inferiority of a novel ultrasound imaging technique, rather than to evaluate a therapeutic intervention.
Locations (1)
Chinese PLA General Hospital
Beijing, Beijing Municipality, China