Endoscopy.
Conditions
Interventions
Intervention 1: Intervention group: Both groups were given fentanyl at a dose of 0.5 micrograms per kilogram. In group A, midazolam was administered intravenously at a rate of 0.5 micrograms per kilog
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: All endoscopic patients Age 20 to 60 years Weight 55 to 85 kg Being in ASA class one or two
Exclusion criteria
Exclusion criteria: Blood pressure history Diabetes Respiratory failure Liver problem Kidney problem Addiction Heart disease Drug allergy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of recovery time in patients between the two groups of midazolam-propofol with midazolam-ketamine in patients undergoing outpatient endoscopy. Timepoint: From the time the procedure was completed to the patient's alertness and appropriate response to questions, recovery time was considered (every 30 seconds, recovery was assessed). Method of measurement: Less than 5 minutes fast, between 5-10 minutes medium and more than 10 minutes slow recovery.;Comparison of hemodynamic changes in the two groups of midazolam-propofol with midazolam-ketamine in patients undergoing outpatient endoscopy. Timepoint: Vital signs (including heart rate, systolic and diastolic blood pressure, and oxygen saturation) before, and during, induction. Method of measurement: Heart rate per minute and systolic and diastolic blood pressure based on millimeters of mercury and arterial blood oxygen saturation.;Age, sex and weight in patients in the two groups of midazolam - propofol with midazolam - ketamine in patients undergoing outpatient endoscopy. Timepoint: On arrival. Method of measurement: Age based on number of years of life and weight based on kg and sex based on phenotype.;Sedation. Timepoint: From the moment of injection and during injection and after waking up. Method of measurement: Based on the Ramsey variable.;Comparison of nausea and vomiting in two groups of midazolam - propofol with midazolam - ketamine in patients undergoing outpatient endoscopy. Timepoint: From the end of the procedure to the time of leaving the recovery. Method of measurement: Visual analoge scale.;Comparison of postoperative pain in patients in two groups of midazolam-propofol with midazolam-ketamine in patients undergoing outpatient endoscopy. Timepoint: At the beginning of the procedure, the end of the procedure and one hour after the end of the procedure. Method of measurement: Ambesh score. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Reza Baqbanian
Ahvaz University of Medical Sciences
Outcome results
None listed