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By invitation only Not applicable NCT07547254

Evaluation of the Efficacy and Safety of Palmitoleic Acid Oil Composition in Preventing Pressure Injuries

No applicable phase (e.g. observational)
Conditions: Pressure Ulcer Prevention

Sponsor: Ruijin Hospital

trial.available_in: БГ
Overview
To evaluate the efficacy and safety of a topical palmitoleic acid (POA) oil composition in preventing PIs and reversing Stage I damage using an integrated physiological monitoring approach.
Description
A prospective, single-center, self-controlled study was conducted enrolling adult inpatients at high risk for PIs (SEM \>0.5) or with existing Stage I PIs from Ruijin Hospital, Shanghai Jiao Tong University School of Medicine . Participants received standard preventive care plus topical POA oil composition (1 mL to sacral area, 4 times daily for 14 days). Primary outcomes included changes in SEM and TcPO₂. Assessments were performed at baseline, day 7, and day 14.
Who can participate
Inclusion Criteria: * Adult inpatients (aged above 18 years). * High risk for sacral pressure injuries, objectively defined by an abnormal hydration status (Sacral Subepidermal Moisture \[SEM\] Delta \> 0.5) at screening. Exclusion Criteria: * Medical contraindications to standard repositioning protocols (e.g., unstable pelvic fractures). * Use of topical medications or advanced prophylactic dressings on the sacrum within 14 days prior to enrollment. * Active peripheral vascular disease significantly impairing local tissue perfusion. * Documented hypersensitivity to the investigational product (POA) or its vehicle components.
Interventions
Topical POA Oil Composition Application for Pressure Injury Prevention
COMBINATION_PRODUCT
Locations 1
China (1)
Ruijin Hospital, Shanghai Jiaotong University School of Medicine
Shanghai , Shanghai Municipality
Technical details
Status
By invitation only
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
01.12.2025
Completion date
01.12.2026
Registry ID
NCT07547254
Source
clinicaltrials.gov
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