RecruitingPhase 2NCT00409435

A Study of Pyridostigmine in Postural Tachycardia Syndrome

Double-Blind, Placebo-Controlled Study of Pyridostigmine in Postural Tachycardia Syndrome


Sponsor

Mayo Clinic

Enrollment

50 participants

Start Date

Oct 1, 2006

Study Type

INTERVENTIONAL

Conditions

Summary

This is a 3-day study comparing pyridostigmine versus placebo in the treatment of postural tachycardia syndrome (POTS). The researchers expect pyridostigmine to improve tachycardia and stabilize blood pressure.


Eligibility

Min Age: 15 YearsMax Age: 55 Years

Inclusion Criteria4

  • Diagnosis of postural tachycardia syndrome using the following criteria:
  • Orthostatic heart rate increment greater than or equal to 30 beats per minute (bpm) within 5 minutes of head-up tilt.
  • Symptoms of orthostatic intolerance. These include weakness, lightheadedness, blurred vision, nausea, palpitations, and difficulty with concentration and thinking.
  • Both criteria must be fulfilled.

Exclusion Criteria6

  • Pregnant or lactating women
  • Presence of failure of other organ systems or systemic illness that could affect autonomic function or the patient's ability to cooperate with the study
  • Hypothyroidism or hyperthyroidism
  • Clinically significant coronary artery disease
  • Medications that could interfere with autonomic testing
  • Previous treatment with pyridostigmine for POTS. Patients must not have taken pyridostigmine in the past month

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Interventions

DRUGpyridostigmine

one 180 mg capsule per day for 3 days

DRUGPlacebo

one capsule per day for 3 days


Locations(1)

Mayo Clinic

Rochester, Minnesota, United States

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NCT00409435


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