Pain.
Conditions
Interventions
Intervention 1: Intervention group: Initially, personal consent is obtained from the patients. Then the patient is placed on the operating bed and appropriate venopuncture is performed and standard m
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age: 18 to 65 years old; ASA I, ASA II; Patients candidate for anesthesia for elective surgery.
Exclusion criteria
Exclusion criteria: Analgesic and opium use 24 hours before the surgery Recent Beta blocker use Allergy to drugs Asthma Patients with history of sever cardiovascular disease, renal disease, hepatic disease, chronic respiratory disease Immuno deficiency Pregnant women Alcohol use in 24 hours before surgery History of seizure
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Nausea. Timepoint: During stay in recovery. Method of measurement: Questionnaire.;Vomiting. Timepoint: During stay in recovery. Method of measurement: Questionnaire. | — |
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Before, during and after injection of Propofol. Method of measurement: VAS score.;Systolic blood pressure. Timepoint: Before, during and after injection of Propofol. Method of measurement: Noninvasive manometer.;Diastolic blood pressure. Timepoint: Before, during and after injection of Propofol. Method of measurement: Noninvasive manometer.;Mean arterial pressure. Timepoint: Before, during and after injection of Propofol. Method of measurement: Noninvasive manometer.;Heart rate. Timepoint: Before, during and after injection of Propofol. Method of measurement: Pulse oximeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFateme Zand
Esfahan University of Medical Sciences
Outcome results
None listed