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Clinical Trials/EUCTR2008-007968-42-FI
EUCTR2008-007968-42-FI
Active, not recruiting
Not Applicable

Patient-controlled sedation vs propofol infusion for ERCP - Patient-controlled sedation for ERCP

Helsinki University Central Hospital0 sitesDecember 23, 2008
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DrugsPROPOFOL-LIPURO 10 mg/ml (1 %)ULTIVA® 1 mg

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Helsinki University Central Hospital
Status
Active, not recruiting
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 23, 2008
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Elective ERCP patients
  • •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
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •under\-age, propofol or/and remifentanyl allergy

Outcomes

Primary Outcomes

Not specified

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