NCT03730272

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Aug 2018

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2018

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

November 1, 2018

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 5, 2018

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2019

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2019

Completed
Last Updated

November 5, 2018

Status Verified

November 1, 2018

Enrollment Period

7 months

First QC Date

November 1, 2018

Last Update Submit

November 1, 2018

Conditions

Post Traumatic PainPost Traumatic Analgesic Treatment

Outcome Measures

Primary Outcomes (2)

  • Worst pain

    NRS scale, 0-10

    0-14 days

  • Average pain

    NRS scale, 0-10

    0-14 days

Secondary Outcomes (1)

  • analgesic methods

    0-14 days

Interventions

analgesic drugs and methodsDRUG

the patient will receive analgesic treatment at the discretion of the physician in charge

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients With any kind of multitrauma, fullfilling inclusion/exclusion

You may qualify if:

  • Patient With trauma, ISS \> 8

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dept of Anesthesiology, Oslo University Hospital, Ullevaal

Oslo, 0407, Norway

RECRUITING

MeSH Terms

Interventions

AnalgesicsMethods

Intervention Hierarchy (Ancestors)

Sensory System AgentsPeripheral Nervous System AgentsPhysiological Effects of DrugsPharmacologic ActionsChemical Actions and UsesCentral Nervous System AgentsTherapeutic UsesInvestigative Techniques

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
professor

Study Record Dates

First Submitted

November 1, 2018

First Posted

November 5, 2018

Study Start

August 1, 2018

Primary Completion

March 1, 2019

Study Completion

November 1, 2019

Last Updated

November 5, 2018

Record last verified: 2018-11

Data Sharing

IPD Sharing
Will not share

Locations

NO(1)