Pain. Pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Intervention group A: Before induction of anesthesia, Dexmedetomidine (0.5 µg/kg) will be slowly injected for 5 minutes. Intervention 2: Intervention group B: Before induction of anest
Sponsors
Bojnourd University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: The patient must be alert The patient must be a candidate for surgery under general anesthesia The patient must not have coagulation problems The patient must not be allergic to Propofol or the other drugs in the study The patient must not have cardiovascular problems
Exclusion criteria
Exclusion criteria: Patients who are addictive or have drug abuse Patients with hepatic failure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Propofol injection pain. Timepoint: Measuring pain in a time interval of 5 to 10 seconds during Propofol injection. Method of measurement: Visual Analog Score (VAS) Form of pain and Numeric rating scale (NRS) For rating the pain. | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean Arterial Pressure (MAP). Timepoint: Before Propofol injection, 5 seconds after Propofol injection, 30 seconds after Propofol injection. Method of measurement: Use of Monitoring device.;Heart Rate (HR). Timepoint: Before Propofol injection, 5 seconds after Propofol injection, 30 seconds after Propofol injection. Method of measurement: Use of monitoring device.;Length of recovery and return from anesthesia. Timepoint: From extubation until the patient regains consciousness. Method of measurement: Time observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Esmaeili
Bojnourd University of Medical Sciences
Outcome results
None listed