Evaluation of the CONDA Stent Retriever in Acute Ischemic Stroke

NARecruitingINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

October 1, 2025

Primary Completion Date

October 1, 2026

Study Completion Date

January 1, 2027

Conditions
Acute Ischemic StrokeLarge Vessel Occlusion
Interventions
DEVICE

Mechanical Thrombectomy using the CONDA Stent Retriever

Intravenous sedation, local or general anesthesia, and anticoagulation management will be administered following the institution's standard of care to ensure subject safety and comfort. These procedures should be applied to the target population at the discretion of the investigator and in accordance with clinical guidelines. The use of CONDA is no different than that established for other CE marked stent retrievers. The use of supportive devices including, long sheaths, guide catheters with our without balloons, distal access catheters, ANA funnel catheter, microcatheters and microwires, along with the CONDA device, will be guided by operator preference and/or center established practices. Operators are required to use these devices according to their labeling and instructions for use.

Trial Locations (2)

1145

NOT_YET_RECRUITING

Semmelweis University Hospital, Budapest

08035

RECRUITING

Vall d'Hebron University Hospital, Barcelona

Sponsors
All Listed Sponsors
lead

Anaconda Biomed S.L.

INDUSTRY