Prospective Longitudinal Monocentric Study to Evaluate the Syde® Digital Endpoint in Patients With Multiple Sclerosis
- Disease/Condition
- Multiple Sclerosis
- Drug/Device/Intervention
- Digital HealthTechnology
- Study type
- Observational
- Intervention type
- other
- Primary sponsor
- SYSNAV
- Location
- Cairo, Egypt
- Phase
- N/A
- Start date
- Apr 25, 2024
- End date
- Nov 30, 2026
- Enrollment
- 61 participants
Longitudinal change of 95th centile of stride velocity
The study aims to assess the validity of real-world activity monitoring by the Syde® wearable
 device in subjects with multiple slclerosis. The Syde® collected data will be compared to
 on-site conventional clinical endpoints for MS pathology (EDSS, FSS and T25FWT). Subjects
 with multiple sclerosis will be assessed every 6 months for 2 years.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06346704
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06346704 through Pure Global AI's free database. This phase not specified trial is sponsored by SYSNAV and is currently Recruitment Completed. The study focuses on Multiple Sclerosis. Target enrollment is 61 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.