search
Back to results

Ventilatory Responses to Hypercapnic and Hypoxic Conditions in Hyperventilants

Primary Purpose

Hyperventilation Syndrome, Hypercapnia, Hypoxia

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Hypercapnic hyperoxic ventilatory response
Hypoxic eucapnic ventilatory response
Sponsored by
Centre Hospitalier Universitaire Saint Pierre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Hyperventilation Syndrome

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • A plethysmography within subject's predicted values
  • A negative metacholine test (no documented allergy)
  • A hyperventilation provocation test result that is consistent with the Nijmegen questionnaire score, confirming either group classification (HVS+ or HVS-)

Exclusion Criteria:

  • Each of the following known or documented conditions: chronic bronchitis (COPD), emphysema, asthma, cardiac disorder, neurological disorder, gastrointestinal disorder, thyroid disorder or psychological/psychiatric disorder
  • Suspicious cardio-pulmonary exercise testing (CPET) with cardiac or respiratory limitation
  • Pregnant women or women in the process of becoming pregnant
  • Persons with a diving practice (amateur or professional),
  • High-level athletes,
  • Active smokers and
  • persons using morphine, and/or barbiturates, and/or anxiolytics and/or sleeping pills

Sites / Locations

  • CHU St Pierre

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

HVS-

HVS+

Arm Description

subjects with no complaint AND a Nijmegen questionnaire score of < 23/64 AND a negative hyperventilation provocation test (criteria revised in 2021) (HVS-)

subjects with complaints AND a Nijmegen questionnaire score of ≥23/64 AND a negative hyperventilation provocation test (criteria revised in 2021) (HVS+)

Outcomes

Primary Outcome Measures

The slope of the ventilatory response to hypercapnia (HCVR)
Ventilation increase (litres/min) per unit increase in PetCO2 (mmHg) using Read's method
The slope of the ventilatory response to hypoxia (HOVR)
Ventilation increase (litres/min) per unit decrease in SpO2 (%) using Read's method
Ventilatory recruitment threshold (VRT) of the HCVR
From the average baseline ventilation and PetCO2, the VRT id the PetCO2 level at which the ventilatory response is activated
Ventilatory recruitment threshold (VRT) of the HOVR
From the average baseline ventilation and SpO2, the VRT is the level of SpO2 at which the ventilatory response is activated

Secondary Outcome Measures

Extrapolated apnoeic threshold of the HCVR
PetCO2 level above which apnoea (zero ventilation) is disrupted, obtained from the extrapolation of the HCVR at the X-axis intersection (when VE=0 l/min)
Dyspnea
Visual analogic scale (VAS) of dyspnea, from 0 (no dyspnea) to 10 (maximal dyspnea)

Full Information

First Posted
October 18, 2021
Last Updated
December 22, 2021
Sponsor
Centre Hospitalier Universitaire Saint Pierre
Collaborators
Université Libre de Bruxelles
search

1. Study Identification

Unique Protocol Identification Number
NCT05189158
Brief Title
Ventilatory Responses to Hypercapnic and Hypoxic Conditions in Hyperventilants
Official Title
Ventilatory Responses to Hypercapnic and Hypoxic Conditions in Hyperventilants
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
October 15, 2021 (Actual)
Primary Completion Date
October 15, 2021 (Actual)
Study Completion Date
October 15, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire Saint Pierre
Collaborators
Université Libre de Bruxelles

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
For almost a century, many hypotheses have converged on the idea of altered chemosensitivity in patients suffering from hyperventilation syndrome (HVS). Given the evolution of current technical equipment and the ability to maximise true positives in HVS ( using the revised hyperventilation provocation test), it seems reasonable to investigate central and peripheral chemosensitivities in HVS subjects.
Detailed Description
In the inter-war period, many medical investigators who studied the hyperventilation syndrome (HVS) had already questioned the chemosensitivity to CO2 in HVS patients, without being able to explore it for all intents and purposes. It was subsequently observed that although HVS is not systematically linked to manifest resting hypocapnia, it is nevertheless systematically correlated with significant variability and complexity of ventilation. This is consistent with the observations of an increased plant gain in HVS, to be related to an increased loop gain (due to instability of controller gain feedback). On the other hand, some authors already noted that, when capnia is chronically compromised in HVS, it can be greatly altered by small, transient and barely perceptible increases in VE: a 10% increase in VE could indeed halve PetCO2, while a sigh would be able to decrease PetCO2 by up to 15mmHg. More recently, teh assumption was made that peripheral chemosensitivity may be impaired in HVS patients. For all these considerations, it seems reasonable to investigate central and peripheral chemosensitivities in identified HVS subjects on the basis of an objective test, such as the induced hyperventilation test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperventilation Syndrome, Hypercapnia, Hypoxia

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HVS-
Arm Type
Other
Arm Description
subjects with no complaint AND a Nijmegen questionnaire score of < 23/64 AND a negative hyperventilation provocation test (criteria revised in 2021) (HVS-)
Arm Title
HVS+
Arm Type
Other
Arm Description
subjects with complaints AND a Nijmegen questionnaire score of ≥23/64 AND a negative hyperventilation provocation test (criteria revised in 2021) (HVS+)
Intervention Type
Diagnostic Test
Intervention Name(s)
Hypercapnic hyperoxic ventilatory response
Intervention Description
The hypercapnic ventilatory response (HCVR) described by Read in 1967 (Read's rebreathing method) is a clinical way to assess the central and peripheric sensitivity to CO2, using a small bag (4-6 l) to achieve prompt equilibrium between the apparatus compartments and the lungs. By rebreathing a hyperoxic mixture with an initial composition of 70% O2, 7% CO2 and 23% N2, this equilibrium is assumed to be achieved after 15 seconds of rebreathing, when the relationship between VE and PetCO2 has become linear.
Intervention Type
Diagnostic Test
Intervention Name(s)
Hypoxic eucapnic ventilatory response
Intervention Description
The hypoxic eucapnic ventilatory response (HOVR) is a clinical way to assess the peripheric chemosensitivity to O2, using a small bag (4-6 l) to rebreathe a gas mixture initially composed of 20% O2, 0% CO2 and Δ% N2. Eucapnia is achieved by the activation of a CO2 reabsorption cell during the course of the test.
Primary Outcome Measure Information:
Title
The slope of the ventilatory response to hypercapnia (HCVR)
Description
Ventilation increase (litres/min) per unit increase in PetCO2 (mmHg) using Read's method
Time Frame
baseline - during the test
Title
The slope of the ventilatory response to hypoxia (HOVR)
Description
Ventilation increase (litres/min) per unit decrease in SpO2 (%) using Read's method
Time Frame
baseline - during the test
Title
Ventilatory recruitment threshold (VRT) of the HCVR
Description
From the average baseline ventilation and PetCO2, the VRT id the PetCO2 level at which the ventilatory response is activated
Time Frame
baseline - during the test
Title
Ventilatory recruitment threshold (VRT) of the HOVR
Description
From the average baseline ventilation and SpO2, the VRT is the level of SpO2 at which the ventilatory response is activated
Time Frame
baseline - during the test
Secondary Outcome Measure Information:
Title
Extrapolated apnoeic threshold of the HCVR
Description
PetCO2 level above which apnoea (zero ventilation) is disrupted, obtained from the extrapolation of the HCVR at the X-axis intersection (when VE=0 l/min)
Time Frame
baseline - during the test
Title
Dyspnea
Description
Visual analogic scale (VAS) of dyspnea, from 0 (no dyspnea) to 10 (maximal dyspnea)
Time Frame
baseline, end of the test

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A plethysmography within subject's predicted values A negative metacholine test (no documented allergy) A hyperventilation provocation test result that is consistent with the Nijmegen questionnaire score, confirming either group classification (HVS+ or HVS-) Exclusion Criteria: Each of the following known or documented conditions: chronic bronchitis (COPD), emphysema, asthma, cardiac disorder, neurological disorder, gastrointestinal disorder, thyroid disorder or psychological/psychiatric disorder Suspicious cardio-pulmonary exercise testing (CPET) with cardiac or respiratory limitation Pregnant women or women in the process of becoming pregnant Persons with a diving practice (amateur or professional), High-level athletes, Active smokers and persons using morphine, and/or barbiturates, and/or anxiolytics and/or sleeping pills
Facility Information:
Facility Name
CHU St Pierre
City
Bruxelles
State/Province
Brabant
ZIP/Postal Code
1000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Ventilatory Responses to Hypercapnic and Hypoxic Conditions in Hyperventilants

We'll reach out to this number within 24 hrs