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Clinical Trials/EUCTR2018-000026-54-SE
EUCTR2018-000026-54-SE
Active, not recruiting
Phase 1

A comparison of sedatives used during gastroscopy, alfentanil vs midazolam

Medicinkliniken, Sjukhuset Lidköping0 sites150 target enrollmentJuly 23, 2018
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ConditionsSedative effect during gastroscopyTherapeutic area: Not possible to specify
DrugsAlfentanil HamelnMidazolam Panpharma

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Sedative effect during gastroscopy
Sponsor
Medicinkliniken, Sjukhuset Lidköping
Enrollment
150
Status
Active, not recruiting
Last Updated
7 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 23, 2018
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Medicinkliniken, Sjukhuset Lidköping

Eligibility Criteria

Inclusion Criteria

  • •Patient between 18\-80 years old
  • •Refererred for policlinical routine gastroscopy
  • •In need of sedative agent
  • •Patient can communicate
  • •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 100
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range 50

Exclusion Criteria

  • •Allergies to any of the used agents
  • •Unable to communicate
  • •Any planned therapuetical interventions
  • •Patient has a suspected alcohol, narcotic och abuse of other drugs, or previous abuse
  • •Pregnant patient
  • •Severe lung disease

Outcomes

Primary Outcomes

Not specified

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