The effect of intravenous laser in burned patients
Not Applicable
Recruiting
- Conditions
- burn with grade 3 and b2 and higher than 20%.Bullous disordersL10-L14
- Registration Number
- IRCT20111121008146N16
- Lead Sponsor
- Vice chancellor for research,Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
patients aged 20-50 years
patients with grade 3 and b2 burns with a higher than 20%
informed consent
Exclusion Criteria
chronic patients with continuous onset drug use
addicted people
pregnant women
Cancer patients
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score of patients. Timepoint: Three to five days after starting treatment every 3 hours. Method of measurement: McGill questionnaire scoring system and VAS mark.
- Secondary Outcome Measures
Name Time Method