Colon polyps
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with Physical Status I and II according American Society of Anesthesiologists ( ASA ); undergoing colonoscopy; aged 18 to 65 years; both gender and Body Mass Index ( BMI ) less than 30; accept to sign the Informed Consent
Exclusion criteria
Exclusion criteria: Patients with a history of allergy to any of the medicines; Body Mass Index greater than 30; refusal to sign the informed conset
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of at least 25% of the number of interventions in the target-controlled infusion group. The following interventions were considered: Propofol dose adjustment by agitation and airway rescue maneuvers if oxygen saturation less than 92% that was verified by pulse oximete during the colonoscopy. | — |
Secondary
| Measure | Time frame |
|---|---|
| Faster awakening in the target-controlled infusion group verified by the time between the end of the colonoscopy and the patient exhibiting OAAS score ( Observer Assessment of Alertness and Sedation ) greater than or equal to 3 | — |
Countries
Brazil
Contacts
Associação Matogrossense de Combate ao Câncer