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Effect Site Controlled, Reaction Time Safeguarded, Patient Maintained Sedation With Propofol in Anxious Patients

NCT00355693 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2006-08-24

No results posted yet for this study

Summary

Whether patient-maintained sedation (the patient controls his/her degree of sedation using a hand-held device) using the drug propofol is safer and more effective when using deteriorating reaction time as an added safeguard against the potential for over sedation in a groups of patients undergoing oral surgery, general dentistry and colonoscopy.

Conditions

  • Oral Surgical Procedures
  • Surgery, Oral
  • Dental Anxiety
  • Surgery
  • Colonoscopy

Interventions

DEVICE

Pump for propofol delivery

Sponsors & Collaborators

  • Equity Partners (University Challenge Fund)

    collaborator OTHER

  • University of Glasgow

    lead OTHER

Principal Investigators

  • Sonia Allam, MB ChB FRCA · University of Glasgow Dept of Anaesthesia

  • Conor P O'Brien, BDS FDS · Glasgow Dental Hospital & School

  • Avril Macpherson, MFDS MSND · NHS Lothian

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-10-31
Completion
2007-02-28

Countries

  • United Kingdom

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 NCT00355693 on ClinicalTrials.gov