Clinical Trials Directory

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

TypeNameDescription
DRUGPropofolafter inicial bolus of propofol, remained sedated with propofol infusion (1-2 mg/kg/min)
DRUGSevofluraneafter 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.