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Pain Prevalence in the Trauma Population

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00552968
First Posted: November 2, 2007
Last Update Posted: October 13, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Lynn Haslam, Sunnybrook Health Sciences Centre
October 31, 2007
November 2, 2007
October 13, 2016
September 2007
September 2008   (Final data collection date for primary outcome measure)
Prevalence of pain at 3 months post traumatic injury. [ Time Frame: 3 months ]
Same as current
Complete list of historical versions of study NCT00552968 on ClinicalTrials.gov Archive Site
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Pain Prevalence in the Trauma Population
Pain Prevalence in the Trauma Population at Sunnybrook Hospital
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.
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.
Observational
Observational Model: Cohort
Time Perspective: Prospective
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Non-Probability Sample
Patients that have been admitted to hospital due to a traumatic injury.
Trauma
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
44
September 2008
September 2008   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
16 Years and older   (Child, Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
 
NCT00552968
208-2007
No
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Lynn Haslam, Sunnybrook Health Sciences Centre
Sunnybrook Health Sciences Centre
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Principal Investigator: Lynn Haslam, RN MN ACNP Sunnybrook Health Sciences Centre
Sunnybrook Health Sciences Centre
October 2016