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Pathophysiology of Orthostatic Intolerance

Pathophysiology of Orthostatic Intolerance

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00608725
Enrollment
260
Registered
2008-02-06
Start date
1996-12-31
Completion date
2029-12-31
Last updated
2025-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tachycardia, Postural Orthostatic Tachycardia Syndrome

Keywords

heart rate, blood pressure, blood volume, sympathetic nervous system, orthostatic tachycardia, orthostatic intolerance, POTS

Brief summary

The purpose of this study is to describe the mechanism of orthostatic intolerance, relying on cardiovascular physiological studies. The syndrome is of undetermined etiology, but the syndrome causes impairment of a number of young adults, females more than males, with symptoms of tachycardia, fatigue, lightheadedness, palpitations, blurred vision, chest discomfort, difficulty concentrating, and dizziness with the upright posture. It is believed that many different pathophysiological processes can give rise to this disorder.

Detailed description

The purpose of this study is to describe the mechanism of orthostatic intolerance, relying on cardiovascular physiological studies. The syndrome is of undetermined etiology, but the syndrome causes impairment of a number of young adults, females more than males, with symptoms of tachycardia, fatigue, lightheadedness, palpitations, blurred vision, chest discomfort, difficulty concentrating, and dizziness with the upright posture. It is believed that many different pathophysiological processes can give rise to this disorder. This is not a clinical trial in the classical sense, but an omnibus protocol to allow for disntinct and personalized pathophysiological testing.

Interventions

RADIATIONDAXOR

131-I-Human Serum Albumin Blood Volume Assessment Kit

PROCEDUREQSweat

Quantitative Sweat Testing

DRUGIntrinsic Heart Rate

Atropine 0.04 mg/kg IV in divided doses Propranolol 0.2 mg/kg IV in divided doses

Sponsors

Satish R. Raj
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Orthostatic intolerance

Exclusion criteria

* Inability or unwillingness to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Physiological abnormalities in orthostatic intolerance1 dayvaried metrics used here

Secondary

MeasureTime frameDescription
quantitative sweat testing2 hourssweat volumes after a QSweat test
blood volume1 dayBlood volume as measured by DAXOR technique
intrinsic heart rate1 hourHeart rate after IV propranolol and IV atropine
residual sympathetic function after pharmacological autonomic blockade3 hourschanges in BP after trimethaphan infusions
norepinephrine spillover3 hourstritiated norepunephrine spillover data

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026