Pain severity induced by propofol injection.
Conditions
Interventions
Intervention 1: In second group (50 patients), 2 cc of Lidocaine 1% before use of Propofol was injected. Intervention 2: The third group (48 patients), received 2 ml of normal saline 0.09% before the
Treatment - Drugs
In second group (50 patients), 2 cc of Lidocaine 1% before use of Propofol was injected
The third group (48 patients), received 2 ml of normal saline 0.09% before the injection of Propofol
Group IV (54 patients) 50 mg Sodium Thiopental before injection of Propofol type Fresenius was injected
Group V (55 patients) also recieved 100µg Fentanyl before injection of Propofol
In first group (53 patients) 2mg/kg of Propofol type Fresenius One percent (MCT/LCT) was injected
Sponsors
Vice chancellor for research, Golestan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 55 Years
Inclusion criteria
Inclusion criteria: inclusion criteria: patient fully satisfied to be studied,between 15-55years-old and ASA1,2 exclusion criteria:A history of drug abuse, alcohol or taking any pain medication during 24 hours before surgery, a history of neurological disease, chronic pain syndrome, thrombofelebit, advanced systemic disease (such as advanced diabetes), and any contraindication based on injection of Propofol lead to patient withdrawal from the study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 24 houre after end of surgery. Method of measurement: Visual analog scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKazem Kazem Nejad
Golestan University of Medical Sciences
Outcome results
None listed