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Management of Antipsychotic Medication Associated Obesity 2 Informed Consent Form, IRB approved 10/13/2011 ClinicalTrials.gov Identifier: NCT01052714 Principal Investigator: Donna Ames, MD Version
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What is support materials - clinicaltrialsgov?
Support materials on ClinicalTrials.gov refer to any additional documents or information provided alongside a clinical trial registration to give more details about the study.
Who is required to file support materials - clinicaltrialsgov?
The party responsible for the clinical trial, usually the sponsor or principal investigator, is required to file support materials on ClinicalTrials.gov.
How to fill out support materials - clinicaltrialsgov?
Support materials on ClinicalTrials.gov can be filled out by uploading documents such as protocols, informed consent forms, and statistical analysis plans through the online submission system.
What is the purpose of support materials - clinicaltrialsgov?
The purpose of support materials on ClinicalTrials.gov is to provide additional transparency and details about a clinical trial to researchers, healthcare professionals, and the public.
What information must be reported on support materials - clinicaltrialsgov?
Support materials on ClinicalTrials.gov must include protocols, informed consent forms, statistical analysis plans, and any other relevant documents necessary for understanding the clinical trial.
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