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Trials / Unknown

UnknownNCT01723319

A Double Blind Randomized Controlled Evaluation of the HBLPADD-coil Transcranial Magnetic Stimulation (TMS) Device - Efficacy and Safety In Subjects With ADHD.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Shalvata Mental Health Center · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Objectives:The purpose of the study is to explore the efficacy and safety of HBLPADD Coil deep brain TMS in subjects with ADHD. Patient Population: The intention is to treat 40 patients diagnosed with ADHD. The patients will be of all racial, ethnic and gender categories, ranging from 18 to 65 years of age. Structure: The study is a randomized, prospective, 5 weeks, double blind study. Blinding: The treatment administrator and the study personnel and patients will be masked to the treatment being administrated. The study group will receive active dTMS treatment and the control group will receive an inactive, sham treatment

Conditions

Interventions

TypeNameDescription
DEVICEHBLPADD coil deep TMS20 daily deep TMS treatment
DEVICEShaminactive treatment

Timeline

Start date
2012-11-01
Primary completion
2013-05-01
First posted
2012-11-07
Last updated
2012-11-07

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01723319. Inclusion in this directory is not an endorsement.

A Double Blind Randomized Controlled Evaluation of the HBLPADD-coil Transcranial Magnetic Stimulation (TMS) Device - Eff (NCT01723319) · Clinical Trials Directory