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Clinical Trials/EUCTR2009-012398-36-FI
EUCTR2009-012398-36-FI
Active, not recruiting
Not Applicable

Patient-controlled sedation with propofol in ERCP:alfentanyl vs remifentanyl

Helsinki University Hospital0 sites75 target enrollmentMay 15, 2009
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ConditionsBilliar tract and pancreatic disoderesMedDRA version: 9.1Level: LLTClassification code 10004676Term: Biliary tract diseaseMedDRA version: 9.1Level: LLTClassification code 10004677Term: Biliary tract disorder NOSMedDRA version: 9.1Level: LLTClassification code 10033616Term: Pancreatic disorder
DrugsUltivaRAPIFENPROPOFOL-LIPURO 10 mg/ml (1 %)

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Billiar tract and pancreatic disoderes
Sponsor
Helsinki University Hospital
Enrollment
75
Status
Active, not recruiting
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 15, 2009
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Helsinki University Hospital

Eligibility Criteria

Inclusion Criteria

  • •\-elective ERCP patients;
  • •\-age 18\-70
  • •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

  • •\-allergy to medcines;
  • •\-dementia,mentally handicapped;
  • •\-grievous liver or kidneys failure;
  • •\-significant heart failure or pulmonary disease

Outcomes

Primary Outcomes

Not specified

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