This is a Clinical study Phase III, Prospective, Randomized, Controlled, Double-blind, Multicenter, National, Non-inferiority.

Its purpose is to determine the noninferiority in efficacy of an investigational product in relation to the product available in the market intended of treating pressure ulcers.

Objectives:

The primary objective of efficacy is the reduction in the area of devitalized tissue based on the photographic record.

The secondary objective is to evaluate:

• formation of granulation tissue;
• the lesion reduction during treatment;
• the healing process of the Pressure Ulcer (PU) range of PUSH;
• the safety of the investigational product.

Study Plan:

• Estimated 92 research participants;
• Aged between ≥ 18 years and ≤ 80 years - both sexes;
• Visits from 1 to 10;
• The maximum lasting period in the study for each research participant will be approximately four weeks.

Evaluations During Study:

Evaluation of Digital Photography: The digital photographic record can provide the relative size of the wound, the tissue color and condition of the surrounding skin. The evaluation of digital photograph of each research participant will be performed by the classification assigned to the decrease of devitalized area and tissue e repair related to the time of healing and observed the formation of granulation tissue and epithelialization from standardized photographs.

Evaluation by PUSH Scales:

In order to provide an evaluation instrument of PUs in Brazil, so that satisfies the simplicity of the use in different clinical scenarios keeping its measurement properties, as previously attested from its original version, the PUSH scale was adapted into Portuguese.

The PUSH Scale considers three parameters or sub - scales of the wound healing process and treatment outcomes: wound area, amount of exudate present on the wound, appearance of the wound.

Retention of Records:

The investigator shall retain all documentation of the study over a period of at least five years from the end of the study. The Sponsor or its designee will provide a list of all documentation which should be kept by the Investigator.

Monitoring:

All aspects of the study will be carefully monitored by Cristália Pharmaceutical Chemicals Ltda. or designated representative of it (Clinical Research Organization - CRO) for evaluations related to good clinical practice and applicable local regulations.

Case Report Forms:

The Monitor will be available if the investigator, or other person of his team, needs information and guidance.

The Monitor of the study should have permanent access to all documentation and it is his obligation to ensure that the Case Report Forms are complete and completed correctly, as well as checking if the data are described according to the source documents, in order to eliminate interferences that may compromise the accuracy of the data generated in the clinical trial.

Audit and Inspections:

Authorized representatives of the Sponsor or designees, regulatory authority or the Ethics Committee of the institution may conduct audits or inspections during or after the study conclusion.

Collecting Data:

The information corresponding to the data of interest from the study will be collected and recorded in Case Report forms provided by Sponsor, and filled from the information contained in the source documents.

Documents are considered sources for study: medical records used by the professional at the time of the visits, diagnostic tests or image.

Informed Consent of Trial:

The Principal Investigator will ensure that the research participant receive verbally and in writing all relevant information about the nature, purpose, the test drug, the possible risks and benefits of the study.

Research participants will be notified that they are free to discontinue the study at any time. That they will have the opportunity to ask questions and to have sufficient time to consider the information received.

Formation of the database:

The database of the study will be assembled with the data from the Case Report Forms. Doubts and discrepancies will generate questions (queries) written to the Principal Investigator.

Inclusion Criteria:

• Both sexes;
• Aged ≥ 18 years and ≤ 80 years;
• Patients hospitalized;
• Patients with leg ulcers in the sacral region with presence of devitalized/ necrotic tissue indicating conservative debridement;
• Understanding, agreement and signing the Informed Consent Form (IFC), and the Authorization Term for the Image Use for publication of results

Exclusion Criteria:

• Infected ulcers;
• Limited ulcers;
• Ulcers with indication for surgical debridement ;
• Periostitis ;
• Obesity II( BMI ≥ 35 ) ;
• Severe malnutrition ( BMI < 16 )
• Hemoglobin (HbA1c ) above the upper limit of normal (ULN ) ;
• Coagulation Factor twice the ULN ;
• Patients with pulmonary emphysema and / or Chronic Obstructive Pulmonary Disease (COPD) ;
• Collagen diseases;
• Psychiatric illnesses;
• Patients using cytotoxic agents ;
• Oncology patients under palliative care ;
• Outpatients ;
• Signs of limb ischemia ;
• Urinary incontinence uncontrolled;
• Fecal incontinence;
• Diarrhea that in the opinion of the investigator , compromise the process of debridement;
• Known allergy from the components of the formulas;
• Pregnancy ;
• Breastfeeding ;
• Local and concomitant use of medications and / or products in the lesion: tyrothricin , gramicidin , tetracycline , hexachlorophene , heavy metals ( mercury, silver) , iodine , potassium permanganate , hydrogen peroxide , soap, detergent.