Neurogenic Orthostatic Hypotension research study with CNS

  • STATUS
    Recruiting
  • sponsor
    Proclara
Updated on 25 March 2021

Summary

Neurogenic Orthostatic Hypotension research study with CNS

Description

This double blind study will evaluate the effect of the drug TD-9855 on participants with Neurogenic Orthostatic Hypotension in improving the symptoms.

Qualified participants receive study-related medical care and study medication or placebo at no cost and may be compensated for time and travel.

Details
Clinical Study IdentifierTX150949
SponsorProclara
Last Modified on25 March 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Ages Eligible for Study: 40-80 Years (Adult)
Genders Eligible for Study: Both
Diagnosed with symptomatic orthostatic hypotension due to Parkinson's disease, multiple system atrophy, or pure autonomic failure, (i.e. neurogenic orthostatic hypotension) At screening, subject must meet the diagnostic criteria of neurogenic orthostatic hypotension
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Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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