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Schizophrenia in San Diego. Migraine in Santa Monica. Mitigating the Effects of Nonadherence in Clinical Trials. Using a Subject Registry to Create a Duplicate-Free Corridor for Conducting Clinical Trials. How Far Are Duplicate Subjects Willing To Go? Subject Registries Reduce Duplicate Subjects Entering CNS Studies. Characteristics of Duplicate Subjects in a Clinical Trial Subject Registry. CNS Sites Cooperate to Detect Duplicate Subjects with a Clinical Trial Subject Registry.

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Schizophrenia in San Diego. Migraine in Santa Monica. Mitigating the Effects of Nonadherence in Clinical Trials. Using a Subject Registry to Create a Duplicate-Free Corridor for Conducting Clinical Trials. How Far Are Duplicate Subjects Willing To Go? Subject Registries Reduce Duplicate Subjects Entering CNS Studies. Characteristics of Duplicate Subjects in a Clinical Trial Subject Registry. CNS Sites Cooperate to Detect Duplicate Subjects with a Clinical Trial Subject Registry.
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CTSDatabase | ctsdatabase.com Reviews

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Schizophrenia in San Diego. Migraine in Santa Monica. Mitigating the Effects of Nonadherence in Clinical Trials. Using a Subject Registry to Create a Duplicate-Free Corridor for Conducting Clinical Trials. How Far Are Duplicate Subjects Willing To Go? Subject Registries Reduce Duplicate Subjects Entering CNS Studies. Characteristics of Duplicate Subjects in a Clinical Trial Subject Registry. CNS Sites Cooperate to Detect Duplicate Subjects with a Clinical Trial Subject Registry.

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Thomas M. Shiovitz, M.D. President. Thomas M. Shiovitz's Resume. Adnan Shawkat - Director of Information Systems. Marlene E. Zarrow, M.Ed. Operations. As a Certified Clinical Research Coordinator at California Neuroscience Research, Marlene has over 8 years of experience coordinating and rating dozens of clinical trials in Psychiatry and Neurology. She has specialized as a psychometrician and educator in CNS studies and has studied extensively on placebo-response issues in clinical trials. Marlene brings...

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.:CTS Database:.

http://www.ctsdatabase.com/concept.html

To date duplicate subjects have only been tracked within some pharmaceutical companies. While such internal data is not shared, best estimates are that at least 5% of subjects are duplicates within the same protocol or program. This is only the tip of the iceberg, as nothing tracks participation across sponsors or indications. Additionally, financial incentives for subjects, sponsors and investigators almost certainly contribute to the problem. Investigator incentives can also be perverse. Site time ...

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Schizophrenia in San Diego. Migraine in Santa Monica. Mitigating the Effects of Nonadherence in Clinical Trials. Using a Subject Registry to Create a Duplicate-Free Corridor for Conducting Clinical Trials. How Far Are Duplicate Subjects Willing To Go? Subject Registries Reduce Duplicate Subjects Entering CNS Studies. Characteristics of Duplicate Subjects in a Clinical Trial Subject Registry. CNS Sites Cooperate to Detect Duplicate Subjects with a Clinical Trial Subject Registry.

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