POTS puzzle: scientists probe blood pressure hormone link
NCT ID NCT00962949
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This completed Phase 1 study at Vanderbilt University looked at how the renin-angiotensin-aldosterone system works in people with POTS, a condition that causes a rapid heart rate and dizziness upon standing. Researchers gave 28 participants (including healthy controls) a one-hour infusion of angiotensin II to measure changes in blood pressure and hormone levels. The goal was to better understand the disease process, not to test a new treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Angiotensin II
- What this could lead to
- If successful, this study could help explain why people with POTS have trouble regulating blood pressure and heart rate when standing.
- What could go wrong
- This is a small, early-phase study with only 28 participants, so results may not apply to everyone with POTS. It is designed to understand the disease, not to test a treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
28 people
The number who actually took part.
- Start date
-
Apr 2009
- Finished
-
Dec 2012
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 64 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of postural tachycardia syndrome by the Vanderbilt Autonomic Dysfunction Center criteria * Age between 18-64 years * Male or females are eligible * Able and willing to provide informed consent * Healthy control subjects with no major medical problem (including postural tachycardia syndrome), free of medications during the study Exclusion Criteria: * Overt cause of postural tachycardia e.g., dehydration * Inability to give or withdraw informed consent * Pregnancy * Hypertension (BP \> 140/90) * Significant co-morbid condition * Other factors which in the investigator's opinion would prevent the subject from completing the protocol
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Vanderbilt University
Nashville, Tennessee, 37232, United States
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