Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
NCT05908760

CO2 Rebreathing in nOH: A Proof-of-Concept Pilot Study

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

28

Participants Needed

1

Research Sites

335 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Neurogenic orthostatic hypotension (nOH) is a chronic condition associated with increased cardiovascular risk and reduced quality of life. On standing, patients with nOH experience a large reduction in blood pressure (BP; at least ≥20/10mmHg, but often much more), which is often accompanied by debilitating symptoms and syncope. A previous study (unpublished) showed that hypercapnia significantly increases standing BP in patients with nOH. Human bodies naturally produce and exhale CO2. Rebreathe devices offer a simple, cost-effective technology to increase arterial CO2. In brief, rebreathe devices work by capturing expired CO2, which is then re-inhaled. The net effect is a transient increase in CO2. A CO2 rebreathing device may offer a novel hemodynamic therapy for patients with nOH. This is a pilot, proof-of-concept study to evaluate a CO2 rebreather to improve blood pressure and orthostatic tolerance in patients with nOH. The hypothesis is that a rebreather will increase CO2 sufficiently enough to improve BP in patients with nOH. Male and female patients (n=28) will be asked to complete two randomized 70° head-up tilt (HUT) tests breathing either room air or using a CO2 rebreather. Hemodynamics (BP, heart rate, stroke volume, brain blood flow) and orthostatic symptoms will be assessed throughout. Breath-by-breath data will include O2, CO2, respiration rate and tidal volume. The primary outcome measure will be the magnitude of the BP response (ΔBP = HUT - Supine) during Room Air vs. Hypercapnia. The primary outcome will be compared between room air and hypercapnia using a paired t-test.

CONDITIONS

Official Title

CO2 Rebreathing in nOH: A Proof-of-Concept Pilot Study

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Male or female
  • Physician diagnosis of Neurogenic Orthostatic Hypotension
  • Non-smokers
  • Able and willing to provide informed consent
  • Ability to travel to Libin Cardiovascular Institute Autonomic Testing Lab at the University of Calgary, Calgary, AB
Not Eligible

You will not qualify if you...

  • Use of medical therapies or medications that interfere with autonomic function testing
  • Pregnant or breast-feeding females
  • Chronic heart failure or severe lung disease causing inability to climb one flight of stairs due to shortness of breath
  • Failure of other organ systems or systemic illnesses affecting autonomic function or ability to cooperate, including dementia, substance abuse, cerebrovascular disease, kidney or liver disease, or nerve damage from surgery
  • Any other factors that would prevent completing the study protocol, such as poor compliance in previous studies

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Calgary

Calgary, Alberta, Canada

Actively Recruiting

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Research Team

J

Jacquie Baker, PhD

CONTACT

A

Angela Qi, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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