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Safety and Efficacy of Propofol Only Sedation in Oral and Maxillofacial Surgery

NCT01227174 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 169

Last updated 2010-10-25

No results posted yet for this study

Summary

The purpose of this study is to determine if the use of propofol only to achieve procedural sedation for the removal of third molars is both safe and effective.

Conditions

  • Procedural Sedation
  • Propofol

Interventions

DRUG

Propofol

Procedural sedation will be achieved using propofol

Sponsors & Collaborators

  • Atlantic Center for Oral and Maxillofacial Surgery

    lead OTHER

Principal Investigators

  • Ben Davis, DDS FRCD(C) · Staff Surgeon at "Atlantic Centre for Oral and Maxillofacial Surgery"

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
15 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • Canada

Study Locations

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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 NCT01227174 on ClinicalTrials.gov