Pivotal Study on the NOVABLOC System for Patients Undergoing Primary Total Knee Arthroplasty

Recruiting

NOVABLOCPivotal Study on the NOVABLOC System for Patients Undergoing Primary Total Knee Arthroplasty

Sponsor:

Synaptrix, Inc.

Code:

NCT07191067

Conditions

Pain

Eligibility Criteria

Sex: All

Age: 21+

Healthy Volunteers: Not accepted

Interventions

Percutaneous radiofrequency electrical nerve stimulation

Non-therapeutic stimulation

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 2026-07-13. This information was provided to ClinicalTrials.gov by Synaptrix, Inc. on 2026-05-29.