The effect of propranolol on post-traumatic stress and clinical outcomes in burn patients

Phase 3

Recruiting

Conditions: burn.
Burn of second degree of chest wall, subsequent encounter
T21.21XD

Registration Number: IRCT20190919044819N2

Lead Sponsor: Qazvin University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 52

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

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.