Comparative Clinical Trial on Neoviderm Skin Emulsion and Connettivina 0.2% Cream to Evaluate the Normalization Process of the Skin and Reduction of Cutaneous Tension and Pain in Patients With Superficial Burns Grade 1 and 2

Status: Recruiting
Location: See location...
Intervention Type: Drug, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

It is a single centre, randomized (set up or distributed in a deliberately random way), open-label (study participants and researchers both know which treatment the patient is receiving), prospective, interventional, post-marketing, controlled (An experiment or clinical trial in which two groups are used for comparison purpose), non-inferiority study (a study that tests whether a new treatment is not worse than an active treatment it is being compared to). The PRIMARY OBJECTIVE is to assess the reduction of skin tension in patients with 1st and 2nd degree superficial burns treated either with Neoviderm Skin Emulsion medical device or Connettivina 0.2% Cream. Neoviderm Skin Emulsion soothes and relieves the skin, promoting its physiological normalization process. It is suitable for adults, children and infants in case of sunburns; 1st degree and 2nd degree superficial burns; superficial ulcers; protection before and after radiotherapy treatment; skin irritation and manifestations involving redness; skin cracks, including recurring ones; desquamative states; erythema; dry skin; small abrasions. It is also indicated only for adults in case of tattoo aftercare and chemical peel.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Healthy Volunteers: f
View:

⁃ The patients should comply with all the following inclusion criteria.

• Adult subjects, adolescents between 11 and 17 years, and children aged ≥ 3 years.

• Both sexes (males and females).

• Subjects or subjects'parents that have given the appropriate writ-ten informed consent (in accordance with local requirements) for the participation in the study at the time of enrolment,

• Subjects with 1st and 2nd superficial burns, either of physical or liquid burns, with an affected cutaneous area ≤ 20% in adults, ≤ 15% in children between 10 and 15 years of age, and ≤ 10% in children between 3 and 10 years and seniors over 65 years of age.

Locations
Other Locations
Italy
UO Dermatologia - Piraccini IRCCS Azienda Ospedaliero-Universitaria di Bologna
RECRUITING
Bologna
Time Frame
Start Date: 2023-04-17
Estimated Completion Date: 2023-12-30
Participants
Target number of participants: 50
Treatments
Experimental: 25 subjects treated with Neoviderm Skin Emulsion
Active_comparator: 25 patients treated with Connettivina 0.2% Cream
Related Therapeutic Areas
Sponsors
Leads: Istituto Ganassini S.p.A. di Ricerche Biochimiche

This content was sourced from clinicaltrials.gov