Non-invasive CTS Device Clinical Trial

NACompletedINTERVENTIONAL
Enrollment

88

Participants

Timeline

Start Date

October 10, 2018

Primary Completion Date

February 28, 2020

Study Completion Date

April 21, 2020

Conditions
Carpal Tunnel Syndrome
Interventions
DEVICE

Study Device

Real study device applied to affected wrist (or higher CTS severity wrist if patient has bilateral CTS) for 8-10 hours daily for 56 days (8 weeks).

DEVICE

Sham Device

Sham device applied to affected wrist (or higher CTS severity wrist if patient has bilateral CTS) for 8-10 hours daily for 56 days (8 weeks). \*Note: participants in the sham group are given the real study device at the end of the Post-Treatment/Follow-up Phase.

Trial Locations (3)

44195

Cleveland Clinic (Lerner Research Institute), Cleveland

90710

South Bay Medical Center, Torrance

92691

Mission Pain & Spine, Mission Viejo

All Listed Sponsors
collaborator

The Cleveland Clinic

OTHER

collaborator

Mission Pain and Spine

OTHER

collaborator

Kaiser Permanente

OTHER

lead

Pressure Profile Systems, Inc.

INDUSTRY

NCT03498287 - Non-invasive CTS Device Clinical Trial | Biotech Hunter | Biotech Hunter