Sedation in patients undergoing endoscopy.
Conditions
Interventions
Intervention 1: Intervethe group: first intervention group was injected with 0.5 mg / kg propofol made by Donk Kong South Node along with 1 mg / kg ketamine made by Trittau, Italy before the intervent
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: All patients aged 18 to 65 years who have referred to Imam Khomeini Hospital in Ahvaz for endoscopic procedure
Exclusion criteria
Exclusion criteria: Patients under 18 or over 65 years of age The patient's unwillingness to participate in the study Patients contraindicated in propofol ketamine or propofol fentanyl
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sedation. Timepoint: Before and during the intervention. Method of measurement: Ramsay sedation scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Before and during the intervention. Method of measurement: Ambesh scor.;Nausea. Timepoint: After the end of the intervention until the exit from recovery. Method of measurement: According to the visual analog scale ( vas )on a ruler that is scaled from zero to ten, zero is equivalent to nausea and ten is equivalent to maximum nausea.;Vomiting. Timepoint: After the end of the intervention until the exit from recovery. Method of measurement: Count the number of vomits. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFateme Jorfi
Ahvaz University of Medical Sciences
Outcome results
None listed