Clinical Trials Logo

Clinical Trial Summary

This study will evaluate the effects on venous blood flow of the investigational device, OsciPulse system, which is an external intermittent limb compression device. The study will enroll healthy human subjects who will have their deep venous blood flow measured by vascular ultrasound during immobility, use of the OsciPulse system, and use of two reference vascular compression devices. Our hypothesis is that the OsciPulse system will create distinct patterns of venous flow, specifically at the site of venous valves, in comparison to the reference compression devices.


Clinical Trial Description

Enrolled healthy subjects will undergo and initial vascular ultrasound imaging procedure to locate a deep venous valve in either the sapheno-femoral junction or femoral trifurcation sites. Once the imaging valve is identified the baseline level of venous flow will be collected in 30 s video clips of 2D color Doppler videos and spectral Doppler. Next, either the OsciPulse device, or one of the two reference therapy devices, will be applied by study personnel according to the device's specific instructions. The subject will wear the device during the capture of 1 spectral Doppler clip and three 30 s 2D color Doppler ultrasound clips on both the left and right leg. Next, the remaining two devices will be applied based on instructions, and vascular ultrasound clips captured for each. Completion of this visit protocol will be the end of the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05087108
Study type Interventional
Source OsciFlex LLC
Contact
Status Completed
Phase Early Phase 1
Start date March 17, 2022
Completion date June 30, 2022

See also
  Status Clinical Trial Phase
Withdrawn NCT03613402 - BRAVO - Betrixaban Registry Using Real Time Observations in Acute Medical Illness to Assess Venous Thrombosis and Bleeding Outcomes
Recruiting NCT05409976 - The GORE® VIAFORT Vascular Stent IVC Study N/A
Completed NCT03015025 - Pharmacogenetic Dosage Algorithm for Acenocoumarol N/A
Completed NCT03911661 - Fearon Algorithm in Warfarin Patient Self-Management N/A
Recruiting NCT05449808 - Evaluation of Thromboprophylaxis Appropriateness in Hospitalized Medical Patients
Withdrawn NCT05246943 - The Correlation of a D-dimer Testing Protocol With Venous Thromboembolism in Surgical Colorectal Patients
Recruiting NCT01339611 - Education Program for Patients Receiving Oral Anticoagulation N/A
Completed NCT04367831 - Intermediate or Prophylactic-Dose Anticoagulation for Venous or Arterial Thromboembolism in Severe COVID-19 Phase 4
Recruiting NCT05711173 - Clonal Hematopoiesis and NETs Formation in Venous Thrombosis (CLODETTE) N/A
Completed NCT04824118 - Clotting Parameters After Medical Abortion
Withdrawn NCT01810237 - Validation of a Novel Dabigatran Based Peri-Operative Bridging Anticoagulation Protocol for Patients on Chronic Warfarin Therapy N/A
Recruiting NCT05489588 - The GORE® VIAFORT Vascular Stent Iliofemoral Study N/A
Terminated NCT04128956 - Aspirin® Plus Rivaroxaban Versus Rivaroxaban Alone for the Prevention of Venous Stent Thrombosis in Patients With PTS Phase 2
Completed NCT04439383 - Risk Stratification for Venous Thromboembolism in Hospitalized Medical Patients
Not yet recruiting NCT06452342 - TRanEXamic Acid to Decrease Heavy Menstrual Bleeding in Individuals Anticoagulated for Venous Thromboembolism Pilot Study Phase 4
Recruiting NCT06087952 - Leiden Thrombosis Recurrence Risk Prevention N/A
Completed NCT05515120 - Rivaroxaban Plus Aspirin to Manage Recurrent Venous Thromboembolic Events Phase 2/Phase 3
Completed NCT03611894 - Comparison of the Radiological Pattern Between the Cerebral Stroke of Arterial and Venous Origin
Completed NCT03835780 - The Risk of Venous Thromboembolism in Systemic Inflammatory Disorders: a United Kingdom (UK) Matched Cohort Study
Recruiting NCT05729464 - Risk Factors and Prediction Model of Cancer-associated Venous Thromboembolism