MedTrace Logo

Study of Comparison of the Effectiveness of Three Diagrams for Sedation in Spinal Anesthesia

NCT02136641 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2014-05-13

No results posted yet for this study

Summary

Objective: To determine the efficacy of sedation schemes to sedation in patients about to undergo spinal anesthesia.

Methods: Pilot study, clinical type, randomized, prospective, single-blind, in which the investigators compared three schemes for sedation in patients undergoing spinal anesthesia.

Keywords: Anesthesia, Spinal Anesthesia, Conscious Sedation, Operating Rooms.

Conditions

  • Anesthesia; Reaction

Interventions

DRUG

Midazolam

Was applied Midazolam 0.03 mg / kg, IV (in the vein), single dose.

DRUG

Midazolam+Fentanyl Combination

Was applied Midazolam 0.015 mg / Kg + Fentanyl 0.8mcg/kg, IV (in the vein), single dose.

DRUG

Midazolam+Ketamine Combination

Was applied Midazolam 0,015 mg / Kg + ketamine 0.25 mg / kg, IV (in the vein), single dose.

Sponsors & Collaborators

  • Universidad de Cartagena

    lead OTHER

Principal Investigators

  • FRANCISCO BERMUDEZ GUERRERO, M.D · Universidad de Cartagena

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2011-12-31
Completion
2012-06-30

Countries

  • Colombia

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02136641 on ClinicalTrials.gov