Myasthenia Gravis Clinical Trials

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TheRapeutic Effect of Different immunosuppressAnts on Non-Thymoma Ocular Myasthenia Gravis: a Real-world Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This study collects the clinical data of new-onset ocular myasthenia gravis (OMG) patients, assesses outcomes and adverse effects of different treatment options, and evaluate risk factors of conversion to generalized MG(GMG).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Age \>18 years and\<75 years;

• Clinical Diagnosis of MG with supporting evidence:

• Patients with ocular muscle type MG who have never received treatment meet one of the diagnoses (1) and (2)-(5): (1) The patient's symptoms involve the extraocular muscles, except for drooping eyelids and diplopia, no other clinical symptoms; (2) unequivocal clinical response to pyridostigmine; (3) positive acetylcholine receptor antibody or musk antibody; (4) decrement of more than 10% in repetitive nerve stimulations study (RNS); (5) the trembling of the single fiber electromyography (SFEMG) is broadened with or without blockade;

• Willingness to sample collection, imaging study and other disease-related examinations and assessments;

• The results of pregnancy tests for female subjects with fertility during the screening period should be negative and effective contraception was used by the patient and her spouse during the study period;

• Patients with informed consent;

• Predicted survival time is longer than 3 years.

Locations
Other Locations
China
Tangdu Hospotal
RECRUITING
Xi'an
Contact Information
Primary
Jun Guo, M.D.
guojun_81@163.com
86-29-8477 8844
Time Frame
Start Date: 2019-11-04
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 200
Treatments
Patients with autoimmune ocular MG
Newly-onset OMG patients who agreed to join the follow-up cohort
Related Therapeutic Areas
Sponsors
Leads: Tang-Du Hospital

This content was sourced from clinicaltrials.gov

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