Clinical trial Recruiting at 1 site Observational Ages 18 to 60

Investigating antibodies in patients with Postural Tachycardia Syndrome

Official title: The Pathophysiological Role of Adrenergic Antibodies in Postural Tachycardia Syndrome (Aims #1&2)

Run by University of Calgary · NCT02673996 · Data updated 2026-11-12

This study is testing if people with Postural Tachycardia Syndrome have more specific antibodies in their blood compared to healthy individuals, which could help us understand the condition better.

More Postural Tachycardia Syndrome trials

Quick facts

Study typeObservational
Ages18 Years to 60 Years
SexAll
Enrollment125 (estimated)
SponsorUniversity of Calgary
Academic / other
Locations1 site (Calgary, Alberta)
StatusRecruiting
StartedJanuary 2016
Main results expectedDecember 31, 2029
Study endsDecember 31, 2030
Registry record updatedMay 5, 2026
Trial IDNCT02673996 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are individuals aged 18-60 who have been diagnosed with Postural Tachycardia Syndrome.

Probably not a fit

Patients with overt causes for postural tachycardia or significant cardiovascular, pulmonary, hepatic, or hematological diseases may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to determine if patients with Postural Tachycardia Syndrome (POTS) have a higher percentage of functional antibodies to adrenergic receptors compared to healthy control subjects. The study will involve patients aged 18-60 who have been diagnosed with POTS and will utilize a rat cremaster artery assay to assess the contractile activity of their sera. The findings could provide insights into the autoimmune aspects of POTS and potentially lead to new treatment approaches.

Why it matters

Potential benefit: If successful, this study could lead to a better understanding of POTS and the development of targeted therapies for patients suffering from this condition.

How similar studies have gone: While this approach is novel in the context of POTS, similar studies investigating autoimmune mechanisms in other conditions have shown promising results.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients who have been previously diagnosed with POTS
* Control subjects (patients not diagnosed with POTS)
* Age between 18 - 60 years
* Males and Females (Give that \>80% of POTS patients are female, we will attempt to enroll a similar percentage of female control subjects)
* Able and willing to provide consent

Exclusion Criteria:

* Smokers
* Overt cause for postural tachycardia, i.e., acute dehydration
* Significant cardiovascular, pulmonary, hepatic, or hematological disease by history or prior testing
* Highly trained athletes
* Subjects with somatization or severe anxiety symptoms will be excluded
* Use of drospirenone (a spironolactone analogue) containing oral contraceptive agent
* Hypertension defined as supine resting BP\>145/95 mmHg off medications or needing antihypertensive medication
* Other factors which in the investigator's opinion would prevent the participant from completing the protocol, including poor compliance during previous studies or an unpredictable schedule
* Unable to give informed consent

Where it's running

  • University of Calgary
    Calgary, Alberta, Canada
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.