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Clinical Trials/NCT03730272
NCT03730272UnknownNot Applicable

The Incidence and Strenght of Pain in Conscious Multitrauma Patients, 0-14 Days After Multitrauma

Oslo University Hospital1 site in 1 country40 target enrollmentStarted: August 1, 2018Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
Worst pain

Study Overview

Brief Summary

To register the perceived pain score during 0-14 days after multitrauma in conscious patients and to register the use (type and dose) of analgesic treatment in the same period.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient With trauma, ISS > 8

Exclusion Criteria

  • •Unconscious patients at admission
  • •patients due for major surgery within 3 hrs of admission
  • •patients primary admitted to other hospitals
  • •not able to communicate in Norewegian

Outcomes

Primary Outcomes

Worst pain

Time Frame: 0-14 days

NRS scale, 0-10

Average pain

Time Frame: 0-14 days

NRS scale, 0-10

Secondary Outcomes

  • analgesic methods(0-14 days)

Investigators

Sponsor
Oslo University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Johan C Ræder

professor

Oslo University Hospital

Study Sites (1)

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