Efficacy of HOFA Versus Hydrocolloid Dressings in the Prevention of PUs in Critically Ill Prone Patients

Recruiting N/A Interventional Study
Prone Position Pressure Ulcer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
262 (estimated)
Sponsor
Puerta de Hierro University Hospital · Other
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About This Trial
Introduction: Prone position (PP) treatment as a rescue strategy for patients with acute respiratory distress syndrome (ARDS) is a technique increasingly used in our daily practice and, as a result of the current health situation due to SARS COV-2, has become the treatment of choice for many patients. Many of the associated complications can be considerably reduced with the implementation of stand…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: All patients in prone position admitted to participating ICU who agree to be included in the study or, if they are unable to communicate, the consent is authorized by their referring family member. Exclusion Criteria: Patients with previous pressure ulcers in the following pro…
Contacts

Leire Maculet-García, RN

+34 618704761

leire.maculet@salud.madrid.org

CONTACT

Montserrat Solís-Muñoz, PhD, MSc, RN

+34 911917457

montserrat.solis@salud.madrid.org

CONTACT