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The purpose of this research is to measure changes in venous blood flow with an air-filled bladder under an intermittent pneumatic compression device cuff (used to prevent deep venous thrombosis) or venous diagnostic device cuff (used to detect deep venous thrombosis). The devices being used in the study are investigational and not FDA-cleared.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Mayo Clinic
Rochester, Minnesota, United States
Start Date
November 15, 2024
Primary Completion Date
December 1, 2026
Completion Date
April 1, 2027
Last Updated
October 28, 2025
500
ESTIMATED participants
Mayo Dopplex ABIlity
DEVICE
Intermittent Pneumatic Compression (IPC)
DEVICE
Lead Sponsor
Mayo Clinic
NCT07102160
NCT06451003
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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