Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
ID05924646

CAlgary SAlt for Postural Orthostatic Tachycardia Syndrome Study

Led by University of Calgary · Updated on 2026-05-07

50

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Postural Orthostatic Tachycardia Syndrome (POTS) is a condition that often causes disabling symptoms and is linked to low blood volume. Researchers are evaluating the effects of a high salt diet compared to a normal salt diet over three months to see if adding salt helps reduce heart rate and improve symptoms. This randomized, placebo-controlled cross-over study aims to understand whether increased salt intake can sustain improved blood volume and reduce symptoms in POTS over a longer period. Participants will follow a moderate salt diet while receiving either additional salt capsules or placebo capsules for six weeks each, switching between treatments in a cross-over design. Salt capsules contain 6 grams of slow-release sodium chloride, taken as 2 grams three times daily. The placebo capsules contain microcrystalline cellulose. Participants will receive three in-lab visits including baseline assessment and evaluations after each diet period, along with urine sodium tests and online surveys. Throughout the study, participants will undergo autonomic function testing including a 10-minute tilt test, blood volume measurements, and blood sample collections with an IV. They will provide 24-hour urine samples to assess salt intake compliance. Researchers will measure heart rate, symptom scores, blood pressure, stroke volume, and plasma catecholamines. Surveys on symptoms and patient experience will be collected. The study involves regular monitoring over the three-month period to assess the effects of salt intake on POTS symptoms and cardiovascular responses.

CONDITIONS

Brief Title

CAlgary SAlt for POTS

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Physician diagnosis of POTS as defined by the CCS Consensus Statement
  • Sustained excessive orthostatic tachycardia of 30 bpm or more within 10 minutes standing
  • No orthostatic hypotension (no decrease greater than 20/10 mmHg within 3 minutes standing)
  • Chronic orthostatic symptoms that improve with lying down
  • Age between 18 and 60 years old
  • Ability to attend the Calgary Autonomic Research Clinic
  • Resident of Canada
Not Eligible

You will not qualify if you...

  • Known cause of postural tachycardia such as acute dehydration or thyroid disease
  • Presence of somatization or severe anxiety symptoms
  • Pregnancy (self-reported)
  • Underlying causes of tachycardia including acute hypovolemia, endocrinopathy, anemia, anxiety, medication effects, recreational drug effects, or prolonged bedrest
  • Factors preventing study completion, including poor compliance in previous studies
  • Use of fludrocortisone
  • Received intravenous saline within 2 months before or planned during the study

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks per treatment arm

Participants take either salt capsules or placebo capsules combined with a moderate salt diet for 6 weeks, followed by a cross-over to the other study arm for another 6 weeks.

3 in-lab study sessions (baseline, end of each treatment arm) and 4 urine sodium collections

Trial Site Locations

Total: 1 location

1

University of Calgary

Calgary, Alberta, Canada, T2N 4Z6

Actively Recruiting

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Research Team

S

Satish R Raj, MD MSCI

T

Tanya Siddiqui, MBBS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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