Actively Recruiting
Acetic Acid 2% Solution for Skin Ulcers
Led by Consorci Sanitari de l'Alt Penedès i Garraf · Updated on 2025-06-26
104
Participants Needed
1
Research Sites
96 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this clinical trial is to assess the effectiveness of acetic acid in patients suffering from chronic cutaneous ulcers with biofilm. The primary question it seeks to address is whether acetic acid (as a 2% topical solution) is superior to the current standard treatment for chronic cutaneous ulcers with biofilm at our center (Prontosan®). Participants will be randomly assigned to receive either the acetic acid solution treatment or the standard current treatment.
CONDITIONS
Official Title
Acetic Acid 2% Solution for Skin Ulcers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 18 years of age
- Receiving continued care at a Consorci Sanitari Alt Penedes i Garraf (CSAPG) hospital or outpatient unit
- Having a cutaneous ulcer with biofilm smaller than 120 cm2 located anywhere except the facial region
- Planning to undergo treatment and follow-up for at least 8 weeks at the study center
- Able to cooperate with all required evaluations
- Providing informed consent by self or legal representative
You will not qualify if you...
- Ulcers with exposed bone tissue
- Ulcers caused by cancer (neoplastic origin)
- Ulcers lasting more than 18 months
- Participation in another clinical trial involving experimental intervention during this trial period or with incompatible visit schedules
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Consorci Sanitari Alt'Pènedes i Garraf
Barcelona, Catalonia, Spain, 08810
Actively Recruiting
Research Team
M
Marta De Vicente
CONTACT
N
Noemí Casaponsa
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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