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Establishment of database and biological sample library for myasthenia gravis

Establishment of database and biological sample library for myasthenia gravis

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000038874
Enrollment
Unknown
Registered
2020-10-08
Start date
2020-11-01
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Myasthenia gravis

Interventions

Myasthenia Gravis Case Group:N/A

Sponsors

Department of Neurology, The Second Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 90 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed by a neurologist as myasthenia gravis (Myasthenia gravis, MG); 2. Agree to receive blood and DNA sample collection; if it is a patient with thymoma, agree to obtain a postoperative thymus specimen; 3. Complete imaging and accept each special evaluation of this research; 4. Voluntarily sign the informed consent form (child patients are signed by their legal representatives; if the child patients can participate in research discussions, they must obtain their own consent).

Exclusion criteria

Exclusion criteria: 1. Severe anxiety, depression and schizophrenia; 2. The Simple Mental State Score (MMSE) for patients >= 14 years old is <= 24 points; 3. Patients with other serious systemic diseases whose expected survival is less than 2 years and cannot complete the follow-up; 4. Those who refuse to participate in the registration survey or are expected to have poor compliance.

Design outcomes

Primary

MeasureTime frame
The generalization rate and risk factors for the generaliza of OMG patients to systemic type at the last follow-up;Change in Quantitative Myasthenia Gravis (QMG) Scores from Baseline to follow up;Change in MG-ADL Scores from Baseline to follow up;Time to reach MMS status in patients receiving immunosuppressive therapy;

Secondary

MeasureTime frame
Cumulative dose/time weighted dose of steroid;Cumulative maintenance time of MMS state;The proportion of side effects in patients receiving immune preparations;Changes of B lymphocytes in patients receiving rituximab treatment;

Countries

China

Contacts

Public ContactChangTing

The Second Affiliated Hospital of Air Force Medical University

changting1981@163.com+86 18066656661

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026