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Clinical Trial

PerQdisc Traditional Feasibility Trial.

NCT: NCT06860867 · RECRUITING

NCT IDNCT06860867
StatusRECRUITING
Start Date2025-01-10
Completion2030-03-31

Brief Summary

This is a traditional feasibility study (TFS) study to evaluate the safety and effectiveness of the PerQdisc. The study is prospective, multicenter, and open label. After a screening period, qualified participants will be enrolled and treated with the PerQdisc. Patients will not be blinded to their treatment. Participants will then complete the safety follow-up period.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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