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Clinical Trials/EUCTR2013-002428-17-DK
EUCTR2013-002428-17-DK
Active, not recruiting
Not Applicable

urse Administered Propofol Sedation vs combined sedation with midazolam/fentanil for colonoscopy in patients with IBD. A randomised controlled trial of satisfaction and adhearence to treatment program. - Propofol vs. standard sedation for colonoscopy. A study on satisfaction

Gastroenheden D, Herlev Hospital0 sitesOctober 22, 2013
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DrugsPropofol B. BraunMidazolam B.BraunFentanyl B. Braun

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Gastroenheden D, Herlev Hospital
Status
Active, not recruiting
Last Updated
10 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 22, 2013
End Date
TBD
Last Updated
10 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Gastroenheden D, Herlev Hospital

Eligibility Criteria

Inclusion Criteria

  • •1\. Elective endoscopy due to IBD or suspected IBD
  • •2\. Willing to be randomised
  • •3\. Provide written informed consent
  • •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 170
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range 30

Exclusion Criteria

  • •1\. Allergy to contents administered
  • •2\. pregnant or nursing
  • •3\. \<18 years of age
  • •4\. Not able to complete questionnaire
  • •5\. Acute condition
  • •6\. severe COPD
  • •7\. \> ASA II
  • •8\. Sleep apnea
  • •9\. Risk of aspiration
  • •10\. Previously difficulty with anesthesia

Outcomes

Primary Outcomes

Not specified

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