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.
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.
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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