Pain Prevalence in the Trauma Population
This study has been completed.
Sponsor:
Sunnybrook Health Sciences Centre
Information provided by (Responsible Party):
Lynn Haslam, Sunnybrook Health Sciences Centre
ClinicalTrials.gov Identifier:
NCT00552968
First received: October 31, 2007
Last updated: October 6, 2011
Last verified: October 2011
| Tracking Information | |||||
|---|---|---|---|---|---|
| First Received Date ICMJE | October 31, 2007 | ||||
| Last Updated Date | October 6, 2011 | ||||
| Start Date ICMJE | September 2007 | ||||
| Primary Completion Date | Not Provided | ||||
| Current Primary Outcome Measures ICMJE |
Prevalence of pain at 3 months post traumatic injury. [ Time Frame: 3 months ] [ Designated as safety issue: No ] | ||||
| Original Primary Outcome Measures ICMJE |
Prevalence of pain at 3 months post traumatic injury. [ Time Frame: 3 months ] | ||||
| Change History | Complete list of historical versions of study NCT00552968 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Pain Prevalence in the Trauma Population | ||||
| Official Title ICMJE | Pain Prevalence in the Trauma Population at Sunnybrook Hospital | ||||
| Brief 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. |
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| Detailed 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. |
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| Study Type ICMJE | Observational | ||||
| Study Design ICMJE | Observational Model: Cohort Time Perspective: Prospective |
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| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Non-Probability Sample | ||||
| Study Population | Patients that have been admitted to hospital due to a traumatic injury. |
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| Condition ICMJE | Trauma | ||||
| Intervention ICMJE | Not Provided | ||||
| Study Group/Cohort (s) | Not Provided | ||||
| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 44 | ||||
| Completion Date | September 2008 | ||||
| Primary Completion Date | Not Provided | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 16 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Canada | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00552968 | ||||
| Other Study ID Numbers ICMJE | 208-2007 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Lynn Haslam, Sunnybrook Health Sciences Centre | ||||
| Study Sponsor ICMJE | Sunnybrook Health Sciences Centre | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Sunnybrook Health Sciences Centre | ||||
| Verification Date | October 2011 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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