Sedation for Endoscopy and Colonoscopy. Anaesthetics and therapeutic gases
Conditions
Interventions
Intervention 1: Intervention group: All patients who are candidates for Endoscopy and Colonoscopy who meet the inclusion criteria in the study and are gastrointestinally prepared are admitted to the e
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients aged 20-65 years are candidates for endoscopy and colonoscopy.
Exclusion criteria
Exclusion criteria: History of drug addiction Psychological disorders History of kidney failure Increased liver enzymes Hemodynamic instability Increased body mass index greater than 35
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Degree of sedation during Endoscopy or Colonoscopy. Timepoint: At the beginning and at minutes 2, 5, 10, and 15 of the procedure. Method of measurement: Modified Observer's Alertness/Sedation scale (MOAA/S). | — |
Secondary
| Measure | Time frame |
|---|---|
| The patient's blood pressure. Timepoint: At the begining and at minutes 2, 5 and 10. Method of measurement: Pneumatic blood pressure monitor.;Heart Rate. Timepoint: At the begining and at minutes 2, 5 and 10. Method of measurement: ECG monitoring.;The patient's arterial oxygen saturation percentage. Timepoint: At the begining and at minutes 2, 5 and 10. Method of measurement: Pulse oximetry.;Recovery time. Timepoint: From the completion of the procedure until the patient's alendronate level reaches more than 8, the patient is recorded as fully conscious and can be discharged. Method of measurement: Alendronate scoring.;Total amount of propofol consumed. Timepoint: At the end of the procedure. Method of measurement: milligrams per minute. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Reza Khajavi
Tehran University of Medical Sciences
Outcome results
None listed