Anaesthesia. Y48.4
Conditions
Interventions
Intervention 1: Intervention group1:Skin stimulation is done 10 minutes before the injection of propofol by an anesthesiologist who is not involved in the study and using a Pro-TENS device, it is plac
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Minimum age 18 years of age and maximum 60 ASA 1or ASA2 group of patients people taking propofol for induction have consent to partipitate in the study
Exclusion criteria
Exclusion criteria: BMI less than 18 or more than 31 ASA grade 3 and above history of liver or kidney disease confusion dementia inability to communicate verbally acute or chronic pain history of allergy to any of the drugs used delivery the weight is more than 80 kg
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Average pain intensity. Timepoint: With the initiation of propofol, the patient is asked to rate her pain intensity from 1 to 10 every 5 seconds until she becomes completely unconscious. Method of measurement: The pain caused by automedit injection is graded based on VAS. 0 = no pain 1= Mild pain, pain that was reported only by the patient's answer to the question, without any change in behavior such as changing the facial expression, withdrawing the hand or shedding tears. 2 = moderate pain, pain that was accompanied by a behavioral symptom in addition to being reported in response to a question, or was reported spontaneously without asking a question. 3 = severe pain, accompanied by a strong vocal response or accompanied by behavioral symptoms The pain caused by the automedit injection is also scored using VAS (visual analog scale) from 0 (no pain) to 10 (worst imaginable pain) and their information is recorded. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBehzad Nazemroaya
Esfahan University of Medical Sciences
Outcome results
None listed