Comparison of nanosilver spray with silorsulfadiazine ointment in burns

Phase 3

Recruiting

• Conditions: Burning.; Calcification and ossification of muscles associated with burns; M61.3

• Registration Number: IRCT20190618043934N4
• Lead Sponsor: Birjand University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 July 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

Having conscious consent of the patient or his close companion to enter the study
Minimum hemoglobin mg / dl 12
Grade 2 and 3 burns
Percentage of thermal burns below 20%
Failure to perform surgery to wash and burn the burn before visiting the hospital
Ability to answer questions

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Wound size. Timepoint: Zero day (hospitalization) and day 7 after hospitalization. Method of measurement: The size of the patient's wound will be measured based on the Betsy Jensen checklist.

Secondary Outcome Measures

Name	Time	Method
Wound infection. Timepoint: 3 and 6 days after hospitalization. Method of measurement: Sampling of the wound by a sterile swab using the Levine technique.