Finding studies
Finding studies
Take this into the appointment.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Lead
Tal Medical, Inc.
The primary objective of this study: * To compare the relative efficacy, as measured by a change in the 6-item Hamilton Rating Scale for Depression (HAM-D6), of 20 and 60 minutes of LFMS compared to sham (placebo) in subjects with treatment resistant depression (TRD). Secondary objectives: * To determine if subjects with TRD may respond to 120 minutes of LFMS. * To determine the persistence of response to LFMS therapy during the observation period. * To evaluate the safety and tolerability of LFMS.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
