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Trial Consent Form for: Intranasal for Improving Cognitive Function in Multiple Sclerosis (NCT02988401) Date of Consent Form 7/17/2020Date: July 17, 2020, Principal Investigator: Ellen M. Dowry, M.D.,
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Read through the trial consent form carefully and make sure you understand all the information provided.
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Fill out all required personal information accurately, such as name, date of birth, and contact details.
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Provide any medical history or current health conditions as requested on the form.
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Who needs trial consent form for?

01
Anyone who is considering participating in a clinical trial needs to fill out a trial consent form.
02
This form ensures that participants are fully informed about the trial procedures, potential risks, and their rights as research subjects.
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Trial consent form is used to document a participant's voluntary agreement to participate in a clinical trial after being informed of all aspects of the trial.
The investigator conducting the clinical trial is responsible for obtaining and filing the trial consent form for each participant.
The trial consent form should be filled out by the participant or their legal representative, with assistance from the investigator or study staff if needed.
The purpose of the trial consent form is to ensure that participants understand the nature of the trial, its potential risks and benefits, and their rights as participants.
The trial consent form must include information about the study's objectives, procedures, risks, benefits, confidentiality, and the participant's rights.
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