Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
NCT05914649

NC Testing in LC & POTS

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

100

Participants Needed

1

Research Sites

327 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients with Postural Orthostatic Tachycardia Syndrome (POTS) and Post-Acute Sequelae of COVID (PASC, or "Long COVID") experience cognitive dysfunction. The investigators will test the hypothesis that 999 mL of IV saline will improve cognitive function in patients with POTS and Long COVID compared to placebo (50 mL of saline).

CONDITIONS

Official Title

NC Testing in LC & POTS

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with Long COVID
  • Positive SARS-COV2 test
  • Symptoms lasting more than 12 weeks after COVID
  • Subjective complaint of brain fog or cognitive dysfunction
  • Patients diagnosed with Postural Orthostatic Tachycardia Syndrome (POTS) from the Calgary Autonomic Investigation and Management Clinic
  • Subjective complaint of brain fog or cognitive impairment
  • Healthy participants without POTS or brain fog
  • Age between 18 and 60 years
  • Both female and male participants
  • Able to give informed consent
Not Eligible

You will not qualify if you...

  • Patients with clear causes for POTS such as dehydration or prolonged bed rest
  • Inability to safely stop medications that could interfere with test results
  • Any other reason the investigator believes would prevent completing the study, including poor compliance or unpredictable schedule
  • Unable to give informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

CONTACT

R

Rasha Hamzeh, RN

CONTACT

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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