Trials / Active Not Recruiting
Active Not RecruitingNCT00608725
Pathophysiology of Orthostatic Intolerance
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 260 (actual)
- Sponsor
- Satish R. Raj · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| RADIATION | DAXOR | 131-I-Human Serum Albumin Blood Volume Assessment Kit |
| PROCEDURE | QSweat | Quantitative Sweat Testing |
| DRUG | Intrinsic Heart Rate | Atropine 0.04 mg/kg IV in divided doses Propranolol 0.2 mg/kg IV in divided doses |
Timeline
- Start date
- 1996-12-01
- Primary completion
- 2029-12-01
- Completion
- 2029-12-01
- First posted
- 2008-02-06
- Last updated
- 2025-10-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00608725. Inclusion in this directory is not an endorsement.