Trials / Completed
CompletedNCT03818048
Inhaled Sevofluran vs Endovenous Propofol for Colonoscopy
Inhaled Sevofluran vs Endovenous Propofol for Sedation Maintenance in Patients Submitted to Colonoscopy
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Centro Medico Docente la Trinidad · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
To compare the anesthetic efficacy of the inhalation versus intravenous technique for maintenance of sedation in patients undergoing endoscopy. A longitudinal, randomized clinical study of 32 patients of both sexes ASA I-III, aged 18-80 years undergoing diagnostic colonoscopy, which was randomly divided into 2 groups. In both, intravenous induction with propofol (2-2.5 mg / kg) was performed, Group A remained sedated with propofol infusion (1-2 mg / kg / min); Group B by inhalation with sevoflurane at a concentration of 2 vol% through a nasal cannula with an oxygen flow.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Propofol | after inicial bolus of propofol, remained sedated with propofol infusion (1-2 mg/kg/min) |
| DRUG | Sevoflurane | after inicial bolus of propofol, remained sedated by inhalation with sevoflurane at a concentration of 2 vol% through a nasal cannula with an oxygen flow. |
Timeline
- Start date
- 2016-01-01
- Primary completion
- 2016-10-01
- Completion
- 2016-12-28
- First posted
- 2019-01-28
- Last updated
- 2019-01-28
Source: ClinicalTrials.gov record NCT03818048. Inclusion in this directory is not an endorsement.