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Clinical Trials/EUCTR2005-003887-48-GB
EUCTR2005-003887-48-GB
Active, not recruiting
Phase 1

Randomised Controlled Trial of patient-controlled sedation for colonoscopy: Entonox versus target-controlled infusion of propofol - RCT of patient controlled sedation for colonscopy

HULL AND EAST YORKSHIRE NHS TRUST0 sites0 target enrollmentOctober 25, 2005
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ConditionsCOLONOSCOPY- NO SPECIFIC MEDICAL CONDITIO
DrugsDIPRIVAN 1%ENTONOX

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
COLONOSCOPY- NO SPECIFIC MEDICAL CONDITIO
Sponsor
HULL AND EAST YORKSHIRE NHS TRUST
Status
Active, not recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 25, 2005
End Date
October 31, 2006
Last Updated
6 years ago
Study Type
Interventional clinical trial of medicinal product

Investigators

Sponsor
HULL AND EAST YORKSHIRE NHS TRUST

Eligibility Criteria

Inclusion Criteria

  • •All patients of both sexes undergoing elective colonoscopy will be recruited
  • •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

  • •1\. Patients with chronic pulmonary disease,
  • •2\. History of colonic resection,
  • •3\. Intolerance to any of the drugs,
  • •4\. Unwilling to enter the trial
  • •5\. ASA class IV,
  • •6\. Allergy to soybeans, eggs,
  • •7\. History of seizure disorder, sleep apnoea, or difficult intubation, a short thick neck, and inability to open mouth widely.

Outcomes

Primary Outcomes

Not specified

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