Status unknownNCT03730272Updated Nov 5, 2018

Occurence of Pain and Use of Analgesic Treatment in Multi-trauma Patients of Intermediate Seveity

An observational study in Post Traumatic Pain and Post Traumatic Analgesic Treatment, sponsored by Oslo University Hospital. Status unknown at 1 site in Norway. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2018-11-05.

Sponsored by Oslo University Hospital · Observational

The sponsor has not verified this record recently (last verified Nov 2018), so the status shown — last known as Recruiting — may be out of date.

Study type: Observational
Model: Cohort
Time perspective: Prospective
Enrollment: 40
Ages: 18 Years to 70 Years
Sex: All

Study 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.

Conditions studied

Post Traumatic Pain
Post Traumatic Analgesic Treatment

In context

Lead sponsor

Oslo University Hospital is the lead sponsor of 810 studies on the registry; 148 are open to participants now.

Counted across the registry records on this site, refreshed daily.

Who can participate

Ages eligible: 18 Years to 70 Years
Sexes eligible: All
Sampling method: Non-probability sample

Study population

Patients With any kind of multitrauma, fullfilling inclusion/exclusion

Inclusion criteria

Patient With trauma, ISS > 8

Exclusion criteria

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

Study design

Observational model: Cohort
Time perspective: Prospective
Enrollment: 40 participants (estimated)
Patient registry: No

Interventions

Druganalgesic drugs and methods
the patient will receive analgesic treatment at the discretion of the physician in charge

What researchers measure

Primary outcomes

Worst pain
NRS scale, 0-10
Time frame: 0-14 days
Average pain
NRS scale, 0-10
Time frame: 0-14 days

Secondary outcomes

analgesic methods
list of drugs (dose and duration) and other analgesic measures
Time frame: 0-14 days

Study locations

1 of 1 sites recruiting

Dept of Anesthesiology, Oslo University Hospital, Ullevaal
Oslo, 0407, Norway
- Johan Raeder, PhD · Contact · johan.rader@medisin.uio.no · 004792249669
Recruiting

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

Updates

Tracking since Sep 25, 2026

No changes since tracking began. The registry record was last updated on Nov 5, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗

Registry details

Key details

Study ID: NCT03730272
Lead sponsor: Oslo University Hospital
Responsible party: Johan C Ræder (professor, Oslo University Hospital) — Principal investigator
First posted: Nov 5, 2018
Start date: Aug 1, 2018
Primary completion: Mar 2019 (estimated)
Completion: Nov 1, 2019 (estimated)
Last update: Nov 5, 2018

Oversight

Data monitoring committee: No
FDA-regulated drug: No
FDA-regulated device: No

View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Other studies from this sponsor

Oslo University Hospital

Start the discussion