burn. Burn of second degree of chest wall, subsequent encounter
Conditions
Interventions
Intervention 1: Intervention group: The intervention in this study includes the administration of propranolol by a physician specializing in burns and after consultation with the advice of a cardiolog
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Able to talking Wounds that are 20 to 50 percent of the total body surface area of TBSA And have wounds that are second and third degree Requires treatment with at least one skin graft surgery Receive propranolol for at least 4 consecutive days 48 hours after hospitalization in the intervention group Satisfaction with participating in data collection
Exclusion criteria
Exclusion criteria: Medical conditions Contraindications to propranolol (beta-blocker contraindication) pregnancy bipolar disorder, head injury cardiopulmonary disease, endocrine and peripheral, asthma, systolic blood pressure less than 90, heart rate 60, inhalation damage 5 years of malignancy, history of AIDS, diabetes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-traumatic stress. Timepoint: At the beginning of the study (before the intervention) and And one month after the intervention. Method of measurement: Impact of Event Scale-Revised. | — |
Secondary
| Measure | Time frame |
|---|---|
| Successful skin grafting. Timepoint: Both groups will be evaluated within two weeks and four weeks after discharge. Method of measurement: Clinical examination in which the evaluation of the success of the transplant means a transplant that is pink in color and firmly attached to the base of the transplant area.;Duration of hospitalization. Timepoint: The first and last day of hospitalization in the ward. Method of measurement: Counting by number of days. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLeili Yekefallah
Qazvin University of Medical Sciences
Outcome results
None listed