Phenotyping of Postural Orthostatic Tachycardia Syndrome (POTS)
University of Texas Southwestern Medical Center · with National Heart, Lung, and Blood Institute (NHLBI) · NCT06292104
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 14+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 350
- US sites recruiting
- 1
- Study start
- March 5, 2024
- Record last updated
- July 17, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This is an observational study to deeply phenotype the disorder of POTS using multiple testing modalities.
Being studied: multimodal diagnostic testing
Conditions: Postural Orthostatic Tachycardia Syndrome
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
POTS Patients
- Age ≥ 14 years, able to provide informed consent (assent with parental consent for age \< 18) and comply with procedures
- Meets consensus criteria for POTS: (1) sustained increase in heart rate ≥ 30 bpm above supine baseline within 10 min of quiet standing or upright tilt (≥ 40 bpm in individuals 12 to 19 years of age) OR sustained upright HR (heart rate) >120 bpm, (2) absence of orthostatic hypotension, (3) symptoms with standing that improve with sitting or lying down, (4) resting supine heart rate \< 100 bpm, (5) orthostatic symptoms present for at least 6 months
- Stable oral medication regimen for at least 14 days
Non-POTS Control Patients
- Healthy women, age 18 - 30 years, able to provide informed consent and comply with study procedures
- Does NOT meet consensus criteria for postural tachycardia syndrome
- No symptoms of orthostatic intolerance or dysautonomia. No history of other major medical disorder
- Resting supine heart rate \< 100 bpm
Exclusion Criteria
None of the following exclusion criteria
- Use of amphetamine-type stimulants, diuretics, selective norepinephrine reuptake inhibitor, anticholinergic medications (including tricyclic antidepressant medications), fludrocortisone, desmopressin in past 14 days
- Use of other autonomic drugs (adrenergic agents, pyridostigmine, droxidopa, triptans, ivabradine) in past 48 hours
- Currently receiving IVIG (Intravenous immunoglobulin), subcutaneous IgG (Immunoglobulin G), or any investigational medication (in past year)
- Infusion of iv fluids in past 7 days
- History or evidence of another condition explaining symptoms or orthostatic tachycardia (e.g. structural heart disease, CSF (Cerebrospinal fluid) hypovolemia, or severe traumatic brain injury)
Recruiting US locations
UT Southwestern Medical Center
Dallas, TX 75208
Site contact: Steven Hopkins · 2146489275 · steve.hopkins@utsouthwestern.edu
Study contacts (from the official record)
- Steve Hopkins · 214-648-9275 · steve.hopkins@utsouthwestern.edu
Similar studies in Texas
All healthy volunteers studies in Texas →- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study of LY4355756 in Healthy Participants
Eli Lilly and Company
- Location
- Dallas, TX
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment
AstraZeneca
- Location
- San Antonio, TX + 1 other US site
- Eligibility basics
- Ages 18–80
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight
Eli Lilly and Company
- Location
- San Antonio, TX
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
Radiprodil in Participants With Hepatic Impairment
GRIN Therapeutics, Inc.
- Location
- DeSoto, TX + 1 other US site
- Eligibility basics
- Ages 18–75