Development of a Prospective Real‐World Data Clinical Registry of Children and Adolescents With Migraine

Objective To develop a multicenter, multistakeholder, prospective clinical registry of children and adolescents with migraine to support the collection of real‐world data of sufficient quality to support regulatory submissions and provide site‐based infrastructure support for future clinical trials....

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Veröffentlicht in:	Headache 2020-02, Vol.60 (2), p.405-415
Hauptverfasser:	Hornik, Christoph P., Gelfand, Amy A., Szperka, Christina L., Pezzuto, Tara, Utevsky, Amanda, Kessel, Shirley, McCune, Susan, Alexander, John J., Benjamin, Daniel K., Cohen‐Wolkowiez, Michael, Victorio, Maria (Cris), Pownhall, Margie, Morgan, Danielle, Ekers, Heather, David Rothner, A, Carabello, Dawn, Szperka, Christina, de Prado, Blanca Marquez, Hershey, Andrew, Bickel, Jennifer, Boorigie, Madeline, Gelfand, Amy, Irwin, Samantha, Saeed, Isra, Kutz, Christen, Ventimiglia, Jodi, Saper, Joel, Gruber, Monica, Hagler, Suzanne, Diaz, Coraly, Quintero, Tami, Rathore, Geetanjali, Aikman, Rachel, Guthrie, Cecilia, Chandler, Zachery, Kerman, Karen, Ryan, Erin, Blume, Heidi, Lee‐Eng, Jacqueline, Arun, Deepa, Stieglitz, Kimberly, Gladstein, Jack, Brengle, Lisa, Patnyiot, Irene, Ross, Judith, Roach, Daniel, Doll, Elizabeth, Thomas, Melissa, Turley, Christine, Nahouraii, Robert, Adams, Julia, Hirtz, Deborah, McHale, Ian
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adolescents Biobanks Child Child, Preschool Children clinical registry Clinical trials Collaboration Data capture Databases, Factual Design Female Follow-Up Studies Headache Health Humans Infrastructure Intersectoral Collaboration Male Migraine Migraine Disorders - diagnosis Mobile Applications Neurological diseases Patients Pediatrics Prospective Studies real‐world data Registries Regulatory agencies regulatory submission Scientific visualization Stakeholder Participation Teenagers United States Visualization
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