WithdrawnNot Applicable

Digital Ischemia Reduction in Critically Ill Patients

Stopped: FDA required a new investigational device disclosure for using the wound vac in a new way

0Started 2023-11

Plain-language summary

Patients requiring high dose pressors (minimum 2) who are unlikely to be weaned off them over 1 day will be identified. Patients will have the device applied to one hand while expectant medical management will continue to the contralateral hand.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients in the cardiac critical care unit/cardiovascular intensive care unit with cardiac pathologies on vasopressor support Exclusion Criteria: * Patients who are not on vasopressor support * Patients under the age of 18

What they're measuring

Incidence of digital ischemia

Timeframe: Day 14

Trial details

NCT IDNCT05661773

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-11

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