U.S., March 7 -- ClinicalTrials.gov registry received information related to the study (NCT06860867) titled 'PerQdisc Traditional Feasibility Trial.' on Feb. 28.
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.
Study Start Date: Jan. 10
Study Type: INTERVENTIONAL
Condition:
Discogenic Low Back Pain
Intervention:
DEVICE: PerQdisc
PerQdisc Artificial Implant
Recruitment Status: RECRUITING
Sponsor: Sp...