Peripheral Tissue Perfusion and Oxygenation in Areas at Risk of Press Ulcer (POTER-OIL) (POTER-OIL)
Pressure Ulcer
About this trial
This is an interventional prevention trial for Pressure Ulcer focused on measuring Hyperoxygenated fatty acid, Olive oil, Prevention, Perfusion and Oxygenation
Eligibility Criteria
PHASE ONE HEALTHY SUBJECTS
Inclusion criteria:
- Healthy volunteers, aged > 20 years without functional limitation.
- BMI of 18.5-25.9 kg/cm2.
- No scars on the heels.
Exclusion criteria:
- Failure to meet all of the above criteria.
- Smokers.
- Consume high levels of alcohol (> 20g/week).
- Tattoos in the measurement areas.
PHASE TWO - PATIENTS
Inclusion criteria:
- Patients aged > 20.
- Patients with risk of deterioration of skin integrity according to Braden score <16.
- no presence of Press Ulcer.
Exclusion criteria:
- Presence of vasoactive drugs in infusion
- Subjects with a pacemaker and/or implanted defibrillator.
- Fever and anaemia with Hb <10 g/dl.
- Hypotension with systolic blood pressure <80 mmHg.
- Transfusion during the last four weeks.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
HEALTHY SUBJECTS
PATIENTS
With healthy subjects in a randomised, open experimental design, in an intrasubject control group (application of HFA / EVOO on one heel, using the contralateral heel as a control and evaluating oxygenation and tissue perfusion in both cases). This intervention would correspond to phase 1
With hospitalised patients and patients from social and health centers an experimental, randomised, open design, also with an intrasubject control group (application of HFA / EVOO on one heel, using the contralateral heel as a control and evaluating oxygenation and tissue perfusion in both cases). This intervention would correspond to phase 2.