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Evaluation of the effectiveness of an ionic silver dressing on a burn victim

Evaluation of the effectiveness of an ionic silver impregnated dressing on a burn victim - ERAPT ERAPT

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
REBEC
Registry ID
RBR-97v22nw
Enrollment
Unknown
Registered
2021-10-13
Start date
2017-10-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burns

Interventions

Intervention group and control group will be formed each with 20 individuals aged 18 to 60 years, of both sexes, with burns of 2 and 3 degrees, in a body area of ??10% to 30% of the body surface. A lo

Sponsors

Faculdade de medicina de Ribeirão Preto
Lead Sponsor
Molnlycke Health Care Brazil
Collaborator

Eligibility

Age
No minimum to 60 Years

Inclusion criteria

Inclusion criteria: Age from 0 to 60 years; Burn of II and III degrees affecting the percentile between 10 to 30 percent of body surface burned; Burn in special areashands and feet; Patients at risk.

Exclusion criteria

Exclusion criteria: known allergy to dressing components;need to change the type of dressing during the study period; Isolated burns on the face, perineum or airways; Electrical burns

Design outcomes

Primary

MeasureTime frame
It is expected to find, after data analysis, lower values ??in relation to pain, discomfort with use and infection rate with the use of dressing impregnated with ionic silver in the treatment of burns compared to the current standard treatment with cream silver sulfadiazine 1%.

Secondary

MeasureTime frame
It is expected to find, after analyzing the data, that the dressing impregnated with ionic silver is cost-effective.

Countries

Brazil

Contacts

Public ContactJuliano Baron Almeida

Faculdade de medicina de Ribeirão Preto

julianoalmeida87@gmail.com5519987018980

Outcome results

None listed

Source: REBEC (via WHO ICTRP)