Do Patients With Chronic Daily Headache Have Continuous Headache or Moments of Headache Relief?
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| Tracking Information | |||||
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| First Received Date ICMJE | April 10, 2009 | ||||
| Last Updated Date | January 4, 2011 | ||||
| Start Date ICMJE | April 2009 | ||||
| Primary Completion Date | June 2009 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Number of Subjects With Daily Headache Who Have Continuous Headache [ Time Frame: Records were reviewed from April 2009 through June 2009 ] [ Designated as safety issue: No ] The number of subjects with Daily Headache who have continuous headache |
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| Original Primary Outcome Measures ICMJE | Not Provided | ||||
| Change History | Complete list of historical versions of study NCT00880425 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
Number of Patient With Daily Headache Who Have Non-continuous Headache [ Time Frame: Records were reviewed from April 2009 through June 2009 ] [ Designated as safety issue: No ] Number of patient with Daily Headache who have non-continuous headache |
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| 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 | Do Patients With Chronic Daily Headache Have Continuous Headache or Moments of Headache Relief? | ||||
| Official Title ICMJE | Do Patients With Chronic Daily Headache Have Continuous Headache or Moments of Headache Relief? | ||||
| Brief Summary | The objective of this study is to determine if patients with chronic daily headache have continuous headache or moments of headache relief. The secondary objective of this study is to determine the period of time patients who have chronic daily headache that is not continuous are headache free. |
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| Detailed Description | This study is a retrospective chart review of all patients over the age of 18 who are seen by the co-investigator during one initial, or routine follow up visit, with the diagnosis of chronic migraine, chronic tension type headache, new daily persistent headache, or chronic post traumatic headache(per International Headache Classification II guidelines6). Patients with the above diagnosis during their routine care are asked five standard questions about their headaches by the co-investigator, and the responses are recorded in the patient's medical record (see question sheet attached). These questions pertain to the patients' health care, and are asked of most patients at the Jefferson Headache center with chronic headache routinely during office visits. |
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| Study Type ICMJE | Observational | ||||
| Study Design ICMJE | Observational Model: Case-Only Time Perspective: Retrospective |
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| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Non-Probability Sample | ||||
| Study Population | Headache clinic patients with diagnosis of Chronic Migraine, New Daily Persistent Headache, Chronic Tension type headache, or chronic post traumatic headache, over age 18. |
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| Condition ICMJE | Chronic Daily Headache | ||||
| Intervention ICMJE | Not Provided | ||||
| Study Group/Cohort (s) |
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| 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 | 45 | ||||
| Completion Date | July 2009 | ||||
| Primary Completion Date | June 2009 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00880425 | ||||
| Other Study ID Numbers ICMJE | SDS/CDH/01 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Stephen Silberstein, Thomas Jefferson University | ||||
| Study Sponsor ICMJE | Thomas Jefferson University | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Thomas Jefferson University | ||||
| Verification Date | January 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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