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Acute Salt Handling in Orthostatic Intolerance

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary and study completion dates: Dec 2027 to Dec 2029v24
  2. Primary and study completion dates: Dec 2025 to Dec 2027v23
  3. Re-verified, no change to tracked fieldsv22
  4. Primary and study completion dates: Dec 2023 to Dec 2025v21
  5. Primary and study completion dates: Dec 2021 to Dec 2023v20
Show 18 earlier versionsHide 18 earlier versions
  1. Re-verified, no change to tracked fieldsv19
  2. Primary and study completion dates: Dec 2019 to Dec 2021v18
  3. Re-verified, no change to tracked fieldsv17
  4. Primary and study completion dates: Dec 2018 to Dec 2019v16
  5. Primary and study completion dates: Dec 2016 to Dec 2018v15
  6. Collaborators: 1 to 2v14
  7. Primary and study completion dates: Dec 2014 to Dec 2016v13
  8. Re-verified, no change to tracked fieldsv12
  9. Primary and study completion dates: Dec 2012 to Dec 2014v11
  10. Re-verified, no change to tracked fieldsv10
  11. Trial status: Recruiting to Active, Not Recruiting
    • Site details revised
    v9
  12. Primary and study completion dates: Dec 2010 to Dec 2012v8
  13. Primary and study completion dates: Dec 2009 to Dec 2010v7
  14. 2 versions Re-verified since Oct 21, 2008, no change to tracked fieldsv5-v6
  15. Secondary endpoint revised
    • Primary endpoint revised
    v4
  16. 2 versions Re-verified since Jan 25, 2008, no change to tracked fieldsv2-v3
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The investigators will test the hypothesis that patients with chronic orthostatic intolerance or postural orthostatic tachycardia syndrome (OI or POTS) will be unable to conserve urinary sodium as compared to healthy control subjects.
Trial Details
NCT Number NCT00581633
Lead Sponsor Vanderbilt University
Collaborators: National Center for Research Resources (NCRR), National Heart, Lung, and Blood Institute (NHLBI)
Conditions
(from sponsor)		 Postural Tachycardia Syndrome, Orthostatic Tachycardia, Orthostatic Intolerance
Related terms Orthostatic Intolerance, Postural Orthostatic Tachycardia Syndrome, Tachycardia
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov