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An exploratory analysis of headache in placebo controlled trials of paroxetine for generalized anxiety disorder
Proposal
1373
Title of Proposed Research
An exploratory analysis of headache in placebo controlled trials of paroxetine for generalized anxiety disorder
Lead Researcher
Jonathan H. Smith, M.D.
Affiliation
University of Kentucky
Funding Source
None.
Potential Conflicts of Interest
None.
Data Sharing Agreement Date
23 March 2016
Lay Summary
Headache is highly prevalent and among the leading causes of neurological disability worldwide. Headache disorders are associated with psychiatric co-morbidity, including generalized anxiety and panic disorders. These latter disorders are most often treated with selective serotonin receptor inhibitors, such as paroxetine. However, paroxetine has been associated with headache as an adverse reaction in 6 to 18% of those treated in clinical trial settings. In the evaluation of an individual presenting with headache, it would be clinically relevant to recognize the subset of individuals who are at greatest risk for headache attributable to an adverse reaction of paroxetine. This would allow the clinician to consider discontinuation of paroxetine in individuals reporting headache where the association is thought to be the strongest, and avoid inappropriate discontinuation of paroxetine in individuals when the association is less likely.
To address this issue, we will perform logistic regression analysis of pooled phase 3 clinical trial data of paroxetine in generalized anxiety disorder. The results will be communicated to headache specialists through abstract and journal submissions.
Study Data Provided
[{ "PostingID": 2536, "Title": "GSK-PAR 29060 637", "Description": "A double-blind, placebo controlled study to evaluate the efficacy and tolerability of paroxetine in patients with Generalised Anxiety Disorder (GAD)
Medicine: paroxetine, Condition: Anxiety Disorders, Phase: 3, Clinical Study ID: PAR 29060 637, Sponsor: GSK" },{ "PostingID": 2537, "Title": "GSK-BRL-029060/RSD-101336/1/CPMS-641", "Description": "A Randomized, Double-Blind, Placebo Controlled, Fixed Dosage Trial to Evaluate the Efficacy and Tolerability of 20 and 40mg/day Paroxetine in Patients with Generalized Anxiety Disorder
Medicine: paroxetine, Condition: Anxiety Disorders, Phase: 3, Clinical Study ID: BRL-029060/RSD-101336/1/CPMS-641, Sponsor: GSK" },{ "PostingID": 2538, "Title": "GSK-PAR 29060/642", "Description": "A Randomized, Double-Blind, Placebo Controlled, Flexible Dosage Trial to Evaluate the Efficacy and Tolerability of Paroxetine in Patients with Generalized Anxiety Disorder
Medicine: paroxetine, Condition: Anxiety Disorders, Phase: 3, Clinical Study ID: PAR 29060/642, Sponsor: GSK" },{ "PostingID": 2542, "Title": "GSK-29060/791", "Description": "A Randomized, Double-Blind, Placebo-Controlled, Flexible Dosage Trial to Evaluate the Efficacy and Tolerability of Paroxetine CR in Patients with Generalized Anxiety Disorder (GAD)
Medicine: paroxetine, Condition: Anxiety Disorders, Phase: 3, Clinical Study ID: 29060/791, Sponsor: GSK" }]
Statistical Analysis Plan
The statistical analysis plan will be added after the research is published.
Publication Citation
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