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Enrolling by Invitation

NCT Number: NCT01370512

Droxidopa / Pyridostigmine in Orthostatic Hypotension

This study is being done to study the combination of pyridostigmine and low-dose Droxidopa for the treatment of orthostatic hypotension.

Enrolling by Invitation

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Mayo Clinic in Rochester

Rochester, Minnesota, 55905, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The presence of OH (fall in systolic BP >=30 mm Hg) is required for this study.
  • Autonomic testing and clinical evaluation demonstrates OH to be of neurogenic etiology.

Exclusion criteria

  • Pregnant or lactating females.
  • Chronic illnesses or the presence of other conditions that potentially involve the CNS or affect autonomic testing. These include congestive heart failure, recent (<6 months) myocardial infarct, severe anemia, diabetes mellitus, alcoholism, malignant neoplasms, amyloidosis, hypothyroidism, sympathectomy, cerebrovascular accidents, and neurotoxins or neuroactive drug exposure.
  • Orthopedic problems or cardiopulmonary disease, sufficient to compromise mobility and activity of daily living.
  • Any known concurrent infection or severe liver or kidney disease.
  • Medications that could affect autonomic function are suspended prior to autonomic testing. Therapy with midodrine, alpha and beta adrenergic antagonists, or other medications that affect autonomic function will be withdrawn 48 hours prior to autonomic evaluations. Fludrocortisone doses up to 0.2 mg per day will be permitted. Stable doses of antidepressants (tricyclics, SSRIs, SNRIs) will also be permitted. The 48h medication withdrawal is reviewed on a case by case basis - if felt unsafe by the investigators, the withdrawal period may be shortened. This will be documented in the study documents.
  • Occasional use of a neuroleptic as an anti-emetic in the past is allowed, but none can have been used within 3 weeks prior to this study.
  • Use of methylphenidate, cinnarizine, reserpine, amphetamine, atypical antipsychotics such as risperidone, olanzapine, and quetiapine or a MAO-A inhibitor within 3 weeks prior to this study.
  • Dementia (DSM-IV criteria - Amer. Psych. Assoc., 1994). The score on the Mini-Mental State Examination must be >24.
  • History of stroke (diagnosed on clinical grounds as an acute deterioration of neurological function typical of a stroke; confirmatory CT or MRI evidence of stroke will be useful but not necessary).
  • History of electroconvulsive therapy.
  • History of brain surgery for Parkinson's disease.

Treatment and study plan

Droxidopa

Drug

100 mg tablets by mouth three times a day

Pyridostigmine

Drug

60 mg tablets by mouth three times a day

Placebo

Other

Looks exactly like the study drug but contains no active ingredients

Primary outcomes

  1. Change in orthostatic diastolic blood pressure

    Time frame: 1 hour after medication administration, 2 hours after medication administration

    diastolic blood pressure measured upon standing reported in mm/Hg

Secondary outcomes

  1. Change in orthostatic systolic blood pressure

    Time frame: 1 hour after medication administration, 2 hours after medication administration

    systolic blood pressure measured upon standing reported in mm/Hg

  2. Change in absolute supine diastolic blood pressure

    Time frame: 1 hour after medication administration, 2 hours after medication administration

    diastolic blood pressure measured while lying flat reported in mm/Hg

  3. Change in absolute supine systolic blood pressure

    Time frame: 1 hour after medication administration, 2 hours after medication administration

    systolic blood pressure measured while lying flat reported in mm/Hg

  4. Change in supine norepinephrine levels

    Time frame: 1 hour after medication administration, 2 hours after medication administration

    measure of serum norepinephrine levels while lying flat reported in pg/mL

  5. Change in orthostatic symptoms

    Time frame: 1 hour after medication administration, 2 hours after medication administration

    measured during tilt study, the patient will be asked to score orthostatic symptoms on a symptom scale ranging from "0" = no symptoms to "10" = near syncope

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Collaborators

  • National Institute of Neurological Disorders and Stroke (NINDS)

Registry information

Official study title

Treatment Trial of Droxidopa and Pyridostigmine to Improve Orthostatic Hypotension Without Aggravating Supine Hypertension

Important dates

Study start
2011
Primary completion
2027
Study completion
2027
First posted
Jun 10, 2011
Registry last updated
Jul 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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