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Neurogenic Orthostatic Hypotension

ENROLL IN THE NEUROGENIC ORTHOSTATIC HYPTOTENSION RESEARCH STUDY

About the Study

If you, or a loved one, are suffering from neurogenic orthostatic hypotension (nOH), there is hope. Medical and non-profit organizations are working tirelessly to find treatments and a cure. Part of the process of discovering effective treatments for neurogenic orthostatic hypotension are clinical trials. These research studies and clinical trials are separated into phases, and are offered to patients with neurogenic orthostatic hypotension after pre-clinical trials and early phase studies are completed. 

A neurogenic orthostatic hypotension clinical trial offers patients the opportunity to receive care from some of the nation’s leading neurologists, and includes treatment and continued monitoring at no cost to the patient, with expenses for time and travel potentially reimbursed as well.

Principle Investigator

Neurologist Leading The Study

The Neurological Research Center at the Fort Wayne Neurological Center is currently enrolling for a clinical study to assess the effectiveness of a new treatment option for patients with neurogenic orthostatic hypotension.

If you are currently suffering from nOH, please review the following qualifications and submit a form below to find out if you qualify for this study. To learn more about participating in a study at the neurological research center read our patient FAQ page or contact us with additional questions.

Inclusion Criteria

You may qualify for the nOH study if you must meet the following criteria.

Condition: Neurogenic Orthostatic Hypotension

Age: 18 years and older

Gender: Male or Female

  • Clinical Diagnosis of symptomatic orthostatic hypotension
  • Able to stand on their own or with limited assistance
  • Written informed consent

Exclusion Criteria

If some of the following apply, you MAY NOT qualify for this study.

  • Known or suspected alcohol or substance abuse disorder in the last 12 months
  • Women who are pregnant, intend to become pregnant during the study, or breast-feeding
  • Untreated closed angle glaucoma
  • Diagnosis of hypertension that requires treatment with antihypertensive medications
  • Any significant uncontrolled cardiac arrhythmia
  • History of myocardial infarction or stroke within the past 2 years
  • Congestive heart failure
  • Any condition in which the investigator believes there may be an increased risk to the patient

See if you qualify for this study

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Movement Disorder Studies - Neurostatic Orthostatic Hypotension

Additional Resources

Resources for Neurogenic Orthostatic Hypotension Patients

We know that a neurogenic orthostatic hypotension diagnosis is a challenging prospect to face. We’re here to help. We want to provide you with every available resource to equip and help you on your health journey. We’ve created a list of organizations that are actively working to find answers, provide information, discover new treatments, and who are relentlessly advocating on your behalf.

NOH Matters is an organization that is raising awareness for neurogenic orthostatic hypotension (nOH). Their website contains a breadth of information on signs and symptoms to potential treatment options.

Visit Website: https://www.nohmatters.com/symptoms-neurogenic-orthostatic-hypotension

Multiple System Atrophy (MSA) is a non-profit coalition committed to improving the quality of life for people experiencing MSA, neurogenic orthostatic hypotension included.  They build awareness, raise funds for research, and offer community for people affected by MSA.

Visit Website: https://www.multiplesystematrophy.org/about-msa/neurogenic-orthostatic-hypotension/

NORD exists to provide information and data on rare diseases. Neurogenic orthostatic hypotension is included in their database and they offer extensive information with links to supporting organizations and medical publications for this disease.

Visit Website: https://rarediseases.org/rare-diseases/orthostatic-hypotension/

Neurogenic Orthostatic Hypotension (nOH) is often found in patients with Parkinson’s disease. If you, or a loved one, are suffering from Parkinson’s disease, this organization is an incredible resource containing everything from detailed information on Parkinson’s Disease to connecting you to local resources in your area.

Visit Website: https://www.apdaparkinson.org