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NCT00675922 Clinical Trial

Study of the Treatment of Burn Wounds With Antimicrobial Topical Soaks

Burn Clinical Trial

— Soaks  

Official title:
Comparing the Use of Sulfamylon 5%, Dakins 0.025%, Cerium, Silver Nitrate 5% and/or Other Topical Antimicrobial Products for the Treatment of Excised and/or Grafted Burn Wounds

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00675922
Other study ID # 95-096
Secondary ID
Status Terminated
Phase Phase 2/Phase 3
First received
Last updated
Start date July 1995
Est. completion date May 2008

Study information
Verified date June 2023
Source The University of Texas Medical Branch, Galveston
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Determine effectiveness of various antimicrobial solutions on burn wounds (infections, wound healing, length of hospital stay).

Description:

Patients were treated with both Sulfamylon soaks and Silver nitrate soaks on different burn areas. These two areas were then compared for incidence (percentage) of infections.

Recruitment information / eligibility
Status Terminated
Enrollment 98
Est. completion date May 2008
Est. primary completion date May 2008
Accepts healthy volunteers No
Gender All
Age group 1 Day to 90 Years
Eligibility Inclusion Criteria: - Burn Injury requiring excisional therapy - Hospitalization required until wounds are closed Exclusion Criteria: - Known hypersensitivity to products - Outpatient treatment for burn injury

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Sulfamylon 5% and Silver Nitrate Soaks
Application of Sulfamylon and Silver Nitrate Solution to burn wound daily

Locations
Country Name City State
United States University of Texas Medical Branch Galveston Texas

Sponsors (1)
Lead Sponsor Collaborator
The University of Texas Medical Branch, Galveston

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Infection Rate Percent of infections following antimicrobial topical treatment with Sulfamylon vs Silver Nitrate Soaks. Acute hospitalization following burn injury: admission to discharge (1-20 weeks)
Secondary Length of Hospital Stay With Various Antimicrobial Solutions for Burn Patients At the request of the study site, this study has been closed. Access to study-related data is unavailable, and the PI is no longer at the institution. Hence, we are unable to submit the results data for this outcome. Although peer-reviewed articles have been located that reference NCT00675922 it is not clear and verifiable (without access to the actual study-related data) what the results for this outcome. Admission to burn unit to discharge
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