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Intravenous (IV) Saline and Exercise in Postural Tachycardia Syndrome (POTS)

This study is ongoing, but not recruiting participants.
Information provided by (Responsible Party):
Satish R. Raj, Vanderbilt University Identifier:
First received: October 21, 2009
Last updated: August 15, 2016
Last verified: August 2016
The investigators will test whether an intravenous infusion of saline (salt water) will improve the exercise capacity in patients with postural tachycardia syndrome (POTS).

Condition Intervention
Postural Tachycardia Syndrome Drug: Saline Other: Placebo

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Intravenous Saline on Exercise Tolerance in Orthostatic Intolerance

Resource links provided by NLM:

Further study details as provided by Satish R. Raj, Vanderbilt University:

Primary Outcome Measures:
  • Difference in VO2max between saline day and placebo day [ Time Frame: Within 2 week ]
    VO2max will be measured hours after saline and after placebo. The 2 interventions will be less than 2 weeks apart.

Secondary Outcome Measures:
  • Exercise capacity/Maximal Load (Watts) during peak VO2 [ Time Frame: Less than 2 weeks ]
    Maximal exercise load will be measured hours after saline and after placebo. The 2 interventions will be less than 2 weeks apart.

  • Cardiac output between exercise tests (inert gas rebreathing technique) [ Time Frame: 2-10 Days between exercise tests ]

Estimated Enrollment: 40
Study Start Date: October 2009
Estimated Study Completion Date: June 2017
Estimated Primary Completion Date: June 2017 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Exercise Post Saline
Saline infusion 1L hours before exercise test
Drug: Saline
IV Normal Saline infused over 30-60 minutes given 3-6 hours PRIOR to exercise study
Other Names:
  • Normal Saline
  • 0.9% saline
Placebo Comparator: Placebo
Placebo given prior to exercise test
Other: Placebo
Placebo x1 lactose tablet


Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Meet diagnostic criteria of Postural Tachycardia Syndrome (POTS) 28
  • Age between 18-65 years
  • Male and female are eligible (although the majority of POTS patients are female).
  • Able and willing to provide informed consent

Exclusion Criteria:

  • Presence of medical conditions that can explain postural tachycardia (e.g., acute dehydration, medications)
  • Pregnancy
  • Other factors which in the investigator's opinion would prevent the subject from completing the protocol.
  • Patients who are bedridden or chair-ridden
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Please refer to this study by its identifier: NCT01000350

United States, Tennessee
Vanderbilt University
Nashville, Tennessee, United States, 37232-2195
Sponsors and Collaborators
Vanderbilt University
Principal Investigator: Satish R Raj, MD MSCI Vanderbilt University
  More Information

Additional Information:
Responsible Party: Satish R. Raj, Assistant Professor of Medicine & Pharmacology, Vanderbilt University Identifier: NCT01000350     History of Changes
Other Study ID Numbers: 090942
Study First Received: October 21, 2009
Last Updated: August 15, 2016

Keywords provided by Satish R. Raj, Vanderbilt University:
orthostatic intolerance
exercise capacity

Additional relevant MeSH terms:
Postural Orthostatic Tachycardia Syndrome
Orthostatic Intolerance
Pathologic Processes
Arrhythmias, Cardiac
Heart Diseases
Cardiovascular Diseases
Primary Dysautonomias
Autonomic Nervous System Diseases
Nervous System Diseases
Neurologic Manifestations
Signs and Symptoms processed this record on June 27, 2017