A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)

Recruiting

A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)

Sponsor:

Boston Scientific Corporation

Code:

NCT04192591

Conditions

Lumbar Spinal Stenosis

Eligibility Criteria

Sex: All

Age: 45+

Healthy Volunteers: Not accepted

Interventions

Superion™ IDS device

Study Details

Eligibility Criteria

Study Design

Interventions and Outcome Measures

Central Contacts and Locations

More Information

Trial information was received from ClinicalTrials.gov and was last updated on 2025-03-31. This information was provided to ClinicalTrials.gov by Boston Scientific Corporation on 2025-03-25.