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Clinical Trials/EUCTR2014-005215-16-BE
EUCTR2014-005215-16-BE
Active, not recruiting
Phase 1

A psychomotor recuperation study after deep sedation for colonoscopy between target controlled and manual titration of propofol.

CHU Brugmann0 sites160 target enrollmentJanuary 15, 2015

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
CHU Brugmann
Enrollment
160
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 15, 2015
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All patients subjected to deep sedation in ambulant care
  • ASA status 1\-3
  • 18\-80 years of age
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 90
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 70

Exclusion Criteria

  • Language barrier.
  • Gastroscopy planned at the same time.
  • Allergies to propofol.
  • All cases were a ‘full stomach’ is suspected (gastric banding)

Outcomes

Primary Outcomes

Not specified

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