Pain after a burn. Acute pain due to trauma
Conditions
Interventions
Intervention 1: Intervention group: The group that receiving lidocaine medicine. Intervention 2: Control group: The group that receiving pethidine drug.
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Informed and free consent to participate in the study 2. Burn severity above 10% 3. Patients admitted to the burn department of Ali Bin Abi Talib Zahedan Hospital
Exclusion criteria
Exclusion criteria: 1. Impaired level of consciousness (GCS < 15) 2. Hemodynamic disturbance during drug injection (SBP = 90 and PR = 60 and RR = 8 and = 90% (O2) and in patients with blood pressure (SBP = 180) or (SBP = 100) ) 3. Use of drugs or alcohol or sedatives or pain relievers in the last 48 hours 4. History of taking MAOI, TCA, SSRI, phenothiazines or sleeping pills 5. Suffering from chronic diseases (congenital or acquired heart diseases, heart failure chronic liver disease, biliary tract diseases, kidney failure and chronic lung disease) according to history and clinical examination 6. Asthma according to history and clinical examination 7. Allergy to lidocaine and pethidine 8. Weight more than 100 kg 9. Lack of consent to enter the study 10. Patient's lack of cooperation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in the amount of pain reported by the patient (pain measured by visual observation). Timepoint: The pain level will be asked and recorded at times 0, 5, 10, 20, 30, and 60 minutes. Method of measurement: VAS criterion. | — |
Secondary
| Measure | Time frame |
|---|---|
| Analgesia onset time in patients receiving lidocaine and IV pethidine. Timepoint: Time after starting to receive lidocaine (in minutes). Method of measurement: Time in minutes. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactmasoumeh abbasnjad
Zahedan University of Medical Sciences
Outcome results
None listed