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NCT00552968 Clinical Trial

Pain Prevalence in the Trauma Population

Trauma Clinical Trial

Official title:
Pain Prevalence in the Trauma Population at Sunnybrook Hospital

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00552968
Other study ID # 208-2007
Secondary ID
Status Completed
Phase N/A
First received October 31, 2007
Last updated October 12, 2016
Start date September 2007
Est. completion date September 2008

Study information
Verified date October 2016
Source Sunnybrook Health Sciences Centre
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Observational

Clinical Trial Summary

The incidence of pain in the post traumatic population is an area that has little to no investigation. This study seeks to determine the incidence and experience of pain in this vulnerable population at different time points - while in hospital, 4 weeks post injury, 3 months post injury.

Description:

This pilot study will be a convenience sample from trauma inpatients at the Sunnybrook Campus. The purpose of the study is twofold: to investigate the prevalence of chronic pain that develops in the trauma population at Sunnybrook, and to see if neuropathic pain exists in this population, acute and/or chronically.

Recruitment information / eligibility
Status Completed
Enrollment 44
Est. completion date September 2008
Est. primary completion date September 2008
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- Over 16 years of age

- ability to read / write in English

- ability to complete an informed consent

Exclusion Criteria:

- history of chronic pain

- unable to give informed consent

- unable to read / write English

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Canada Sunnybrook Health Sciences Centre Toronto Ontario

Sponsors (1)
Lead Sponsor Collaborator
Sunnybrook Health Sciences Centre

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Prevalence of pain at 3 months post traumatic injury. 3 months No
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