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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00880425
Other study ID # SDS/CDH/01
Secondary ID
Status Completed
Phase N/A
First received April 10, 2009
Last updated January 4, 2011
Start date April 2009
Est. completion date July 2009

Study information

Verified date January 2011
Source Thomas Jefferson University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date July 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with Chronic Migraine, New Daily Persistent Headache, Chronic Tension type headache, or chronic post traumatic headache seen at the Jefferson Headache Center.

Exclusion Criteria:

- Subjects under age 18.

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Jessica Ailani Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Thomas Jefferson University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Subjects With Daily Headache Who Have Continuous Headache The number of subjects with Daily Headache who have continuous headache Records were reviewed from April 2009 through June 2009 No
Secondary Number of Patient With Daily Headache Who Have Non-continuous Headache Number of patient with Daily Headache who have non-continuous headache Records were reviewed from April 2009 through June 2009 No
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