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

Post Traumatic Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03730272
• Other study ID #: Trauma.pain.Gyda
• Status: Recruiting
• Start date: August 1, 2018
• Est. completion date: November 1, 2019

Study information

• Verified date: November 2018
• Source: Oslo University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: November 1, 2019
• Est. primary completion date: March 2019
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

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

Related Conditions & MeSH terms

• Post Traumatic Analgesic Treatment
• Post Traumatic Pain

Intervention

Drug:
• analgesic drugs and methods
the patient will receive analgesic treatment at the discretion of the physician in charge

Locations

Country	Name	City	State
Norway	Dept of Anesthesiology, Oslo University Hospital, Ullevaal	Oslo

Sponsors (1)

Lead Sponsor	Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Worst pain	NRS scale, 0-10	0-14 days
Primary	Average pain	NRS scale, 0-10	0-14 days
Secondary	analgesic methods	list of drugs (dose and duration) and other analgesic measures	0-14 days