ClinicalTrials.gg
RecruitingNCT06866652MyaRESPUpdated May 8, 2026

Evaluating Dyspnea in Autoimmune Myasthenia Gravis "Why am I Short of Breath?"

An observational study in Myasthenia Gravis and Dyspnea, sponsored by Institut de Myologie, France. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-08.

Sponsored by Institut de Myologie, France · Observational

From the registry’s dates

  • Started Apr 2026; still recruiting 7 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

Individuals with MG (IwMG) experience shortness of breath that may be activity-related, occur at rest and even happen during sleep. Dyspnea is a complex, multidimensional and multifactorial symptom involving sensory perception, cognition and emotion. Identifying the cause(s) of dyspnea in MG may assist in finding therapeutic strategies, reducing discomfort, improving QoL and potentially limiting respiratory deterioration and incidence of MG crisis.

Read the detailed description

MYaResp is a prospective observational, cross-sectional study to evaluate dyspnea in adults with autoimmune myasthenia gravis.

Study aims include to:

  • Describe the characteristics of dyspnea in IwMG
  • Understand contributing factors and factors associated with dyspnea in IwMG including the relationship between patient-reported dyspnea, disease severity and functional limitations.
  • Determine the most effective tests to identify the causes and contributing factors of dyspnea
02

Conditions studied

  • Myasthenia Gravis
  • Dyspnea

Keywords

  • dyspnea
  • breathlessness
  • respiratory
03

In context

Myasthenia Gravis

330 studies on the registry are indexed under Myasthenia Gravis; 144 are open to participants now.

This study's planned enrollment of 50 is below the median of 130 across 105 observational studies indexed under Myasthenia Gravis.

Browse Myasthenia Gravis studies →

Lead sponsor

Institut de Myologie, France is the lead sponsor of 30 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Age ≥18 Confirmed diagnosis of autoimmune MG Shortness of breath in daily life: score 1 or 2 on the respiration item on the MG- activities of daily living score

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥18
  • Confirmed diagnosis of MG
  • Shortness of breath in daily life: score 1 or 2 on the respiration item on the MG- activities of daily living score
  • Signed consent form
  • Affiliated to or beneficiary of a social security scheme

Exclusion criteria

Exclusion Criteria:

  • Known Pregnancy
  • Known respiratory disorder (other than MG)
  • Recent (within past 4 weeks) respiratory infection
  • Current MG crisis or exacerbation (necessitating increase in MG medication \&/or hospital admission)
  • No dyspnea - score 0 or 3 on the respiration item on the MG- activities of daily living score
  • Severe cognitive impairment/guardianship
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Dyspnea questionnaires

    Dyspnea-12

    Time frame: baseline

Secondary outcomes

  1. cardiopulmonary exercise test

    cycle ergometer

    Time frame: baseline

  2. Polysomnography

    evaluation of sleep disordered breathing

    Time frame: baseline

  3. Functional measures

    6 minute walk test

    Time frame: baseline

  4. Quality of life questionnaires

    Revised version of the myasthenia gravis quality of life questionnaire (Burns, French validation Birnbaum)

    Time frame: baseline

  5. Anxiety and depression

    Hospital Anxiety and Depression Scale

    Time frame: baseline

Other outcomes

  1. impact of myasthenia in daily living

    impact of myasthenia in daily living score

    Time frame: baseline

  2. Respiratory pressures

    inspiratory and expiratory pressures

    Time frame: baseline

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06866652
Lead sponsor
Institut de Myologie, France
Collaborators
APHP
Responsible party
Sponsor
First posted
Mar 10, 2025
Start date
Apr 8, 2026
Primary completion
Jun 2028 (estimated)
Completion
Jun 2028 (estimated)
Last update
May 8, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion