About this trial
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.
Eligibility criteria
Qualifiers
Venous ultrasound study to evaluate for lower extremity DVT unilateral and/or bilateral within previous 72 hours.
Disqualifiers
Patients with inaccessible target limb (ultrasound limb) due to bandages (wound, burn, lesion, etc) or cast.
Patients with leg trauma, fracture, above or below knee amputation, or other condition in which compressing on the calf is medically inappropriate or not possible.
Patients unable to provide informed written consent.
Trial design
Treatments tested in this trial
- Mayo Dopplex ABIlity
- Intermittent Pneumatic Compression (IPC)