Actively Recruiting
Patient Observation With Environmental and Wearable Sensors in Myasthenia Gravis
Led by Heinrich-Heine University, Duesseldorf · Updated on 2024-06-04
20
Participants Needed
1
Research Sites
78 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This observational study seeks to investigate the underlying processes of myasthenia gravis by employing multimodal monitoring techniques. By integrating digital biomarkers alongside clinical monitoring, we aim to enhance the detection of disease activity and establish correlations between digital measures, clinical scores and various questionnaires including sores on quality of life, sleep quality or activities of daily living. Primarily including patients treated with newly approved drugs, it aims at improving and monitoring the efficacy and safety of treatment and allowing a more individualized treatment.
CONDITIONS
Official Title
Patient Observation With Environmental and Wearable Sensors in Myasthenia Gravis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Formal diagnosis of generalized Myasthenia Gravis with at least one of the following: response to acetylcholinesterase inhibitors, evidence of pathological decrement or elevated jitter, or presence of MG-typical antibodies (AChR, LRP4, MuSK, Titin) or other diagnosed Myasthenic Syndrome
- Age 18 years or older
- Use of a smartphone with Android 8.1 or higher, or iOS 12.3 or higher
- Able to provide informed consent as judged by the investigator
You will not qualify if you...
- Unable or unwilling to give informed consent
- Unable or unwilling to use the smartphone app
- Any significant comorbidity that might interfere with study participation as judged by the investigator
- Only having ocular symptoms of Myasthenia Gravis (ocular myasthenia gravis)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Heinrich-Heine University, Duesseldorf
Düsseldorf, Germany
Actively Recruiting
Research Team
M
Marc Pawlitzki, PD Dr. med.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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