The Symani Restore Study for Moyamoya Disease
This study is looking at the safety and effectiveness of the Symani Surgical System for adults with Moyamoya disease. Moyamoya disease is a rare, progressive cerebrovascular disorder caused by blocked arteries at the base of the brain. The Symani Surgical System is a device used during surgery. To join, you must be over 18, have Moyamoya disease with minor to moderate symptoms needing surgery, and agree to have the surgery with the Symani system. The main way researchers will know if the treatment is successful is by looking at CT imaging results after 6 months. The study plans to enroll 15 participants, but its current status is unclear.
- Study design
- This is an interventional study. It plans to enroll 15 adult participants.
- What's involved
- Patients must agree to have surgery and anesthesia. They must also agree to sign an Informed Consent Form.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for at least 6 months, as CT imaging is measured at that time point.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
The Symani Restore Study
At a glance
Conditions
NCT07140731
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Jacobs Institute
Buffalo, New Yorkno site contact published
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- CT Imaging6 Months
Stable cerebral perfusion confirmed with CT Imaging