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Clinical Trial Summary

The evidence is insufficient to determine whether the types of dressings containing silver differ in time / proportion for complete wound healing and pain. We will analyze the cost-effectiveness of these dressings in outpatients, considering the service provided by the Brazilian National Public Health System.


Clinical Trial Description

Randomized, single-center, single-blinded, controlled clinical trial. Adult patients (age between 18 and 65 years), regardless of sex, with second degree burns treated in outpatient regimen will be randomized (1:1) into two groups: 1% silver sulfadiazine and nanocrystalline silver. Primary outcome: - Proportion of lesions completely epithelialized within 15 days. Secondary outcomes: - Time in days for complete epithelialization of the burned areas; - Number of dressing changes; - Level of pain associated with the application and removal of the dressings; - Direct medical and non-medical costs; - Need for surgery; - Incidence of infection; - Presence of local adverse reactions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02108535
Study type Interventional
Source University of Sorocaba
Contact
Status Completed
Phase Phase 4
Start date November 2013
Completion date October 2014

See also
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Recruiting NCT03048188 - Manuka Honey in Second- and Grafted Third-degree Burns N/A
Completed NCT03530150 - Pirfenidone and Its Role in Burn Wound Healing Phase 2