Overview

Inhaled Sevofluran vs Endovenous Propofol for Colonoscopy

Status:
Completed
Trial end date:
2016-12-28
Target enrollment:
0
Participant gender:
All
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.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Centro Medico Docente la Trinidad
Treatments:
Propofol
Sevoflurane
Criteria
Inclusion Criteria:

- Age between 18 and 80 years

- physical status I, II and III according to the criteria of the American Society of
Anesthesiology (ASA)

- patients who are going to undergo diagnostic colonoscopies

- patients who signed the informed consent

Exclusion Criteria:

- Allergy or hypersensitivity to some of the reference drugs in the study

- patients with proven liver disease

- suspicion or confirmation of pregnancy

- antecedent or risk of malignant hyperthermia

- fasting less than 8 hours

- patients with psychic disorders or mental incapacity that make it difficult to
understand their participation in the study

- patients who have acute illnesses that compromise their health for which the study
cannot be performed