Assessing the result of dermal graft without suture fixation in burn patients

Phase 2

• Conditions: Condition 1: Burn. Condition 2: Burn. Condition 3: Burn.; Burn and corrosion of head and neck; Burn and corrosion of trunk; Burn and corrosion of shoulder and upper limb, except wrist and hand

• Registration Number: IRCT201610029014N118
• Lead Sponsor: Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

burn patients who are candidate for dermal graft.
Exclusion criteria: Sensitivity to anesthesia medications; contraindication of general or spinal anesthesia.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Assessing the result of dermal graft without suture fixation. Timepoint: 5 days after surgery. Method of measurement: through physical examination.

Secondary Outcome Measures

Name	Time	Method
Assessing local hematoma or bleeding at surgical location. Timepoint: 5 days after surgery. Method of measurement: through physical examination.