Status:

COMPLETED

Peripheral Dopamine in Postural Tachycardia Syndrome

Lead Sponsor:

Vanderbilt University

Conditions:

Postural Tachycardia Syndrome

Orthostatic Intolerance

Eligibility:

All Genders

18-60 years

Phase:

PHASE2

PHASE3

Brief Summary

The purpose of the proposed research is to determine how changes in kidney dopamine (DA) activity influence urinary sodium excretion. We will decrease DA activity in the kidney by inhibiting DA synthe...

Detailed Description

We will determine whether inhibition of renal dopamine formation by carbidopa administration leads to a decrease in urinary excretion of dopamine and sodium and whether the response differs in POTS an...

Eligibility Criteria

Inclusion

  • Patients diagnosed with POTS by the Vanderbilt Autonomic Dysfunction Center based on the following stringent criteria: 1) history of daily orthostatic symptoms for at least 6 months; 2) increase in heart rate (HR) of at least 30 bpm with standing or a standing HR of at least 120 bpm; 3) absence of orthostatic hypotension (defined as a fall in blood pressure (BP)\>20/10 mm Hg); and 4) absence of conditions, such as dehydration, substantial weight loss, or systemic illnesses, that could provoke orthostatic intolerance
  • Upright plasma NE at least 600 pg/mL in patients
  • Non-smoking
  • Free of medications with the potential to influence BP
  • Able and willing to provide informed consent -

Exclusion

  • Overt cause for postural tachycardia (such as acute dehydration)
  • Significant cardiovascular, pulmonary, hepatic, or hematological disease by history or screening results
  • Positive urine b-hcg pregnancy test
  • Evidence of cardiac structural disease (by clinical examination or prior echocardiogram)
  • Hypertension defined as a BP\>145/95 (off medications) or need for antihypertensive medications
  • Evidence of significant conduction system delay (QRS duration \>120 ms) on electrocardiogram
  • Inability to give, or withdraw, informed consent

Key Trial Info

Start Date :

May 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2021

Estimated Enrollment :

32 Patients enrolled

Trial Details

Trial ID

NCT00685919

Start Date

May 1 2008

End Date

December 1 2021

Last Update

January 24 2022

Active Locations (1)

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1

Vanderbilt University Medical Center

Nashville, Tennessee, United States, 37232