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Prevalence of Rest Dyspnea and Impact of Non Invasive Ventilation on Breathing Sensations in CCHS Patients

Prevalence of Rest Dyspnea and Impact of Non Invasive Ventilation on Breathing Sensations in Patients With Congenital Central Hypoventilation Syndrome

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04447196
Acronym
DyspnOndine
Enrollment
20
Registered
2020-06-25
Start date
2021-12-15
Completion date
2022-10-01
Last updated
2021-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CCHS, Congenital Central Hypoventilation Syndrome, Dyspnea

Brief summary

Congenital central hypoventilation syndrome (CCHS) is a neuro-respiratory disease characterized by lifethreatening sleep-related hypoventilation involving an alteration of CO2/H+ chemosensitivity. This suggests cortical activity during awakening to maintain breathing. Cortical activity to keep breathing is usually associated with breathing discomfort ; this is the case in healthy subjects under non invasive ventilation (NIV) or with expiratory charge as well as in patients with amyotrophic lateral sclerosis. This can suggest that CCHS may be breathless at rest and this discomfort could be reduced by NIV. The objective is to evaluate dyspnea with a multi dimensional score, MDP, in CCHS patient at rest in every day life and during 1H session of NIV. The investigators will perform a prospective, including 20 CCHS patients. MDP scores will be measure before and after 1H-non invasive ventilation as well as a visual scale of 100mm in order to evaluate variation of breathing discomfort before/after NIV. The investigators expect that CCHS patients don't have rest dyspnea but NIV would improve breathing discomfort that would mean they have latent rest dyspnea.

Interventions

OTHERMDP

Multi dimensional dyspnea profile scores at rest and during non invasive ventilation

Sponsors

Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients with CCHS confirmed by genetic test * patients with long term non invasive ventilation * no recent condition that could impact breathing sensations such as infection, pulmonary embolism, heart failure

Exclusion criteria

* pregnancy * phrenic nerve stimulation

Design outcomes

Primary

MeasureTime frameDescription
Immediate unpleasantness corresponding to A.1 item of the multidimensional dyspnea profileChange in MDP score between baseline and after 1 hour of NIVMeasure MDP scores before and after NIV

Countries

France

Contacts

Primary ContactMARLENE BRET
marlene.bret@aphp.fr0698674449

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026