NCT02376946 - Third Molar Extraction and Pulsed Electromagnetic FieldTherapy | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

August 31, 2015

Study Completion Date

August 31, 2015

Conditions

Postoperative Edema and Pain

Interventions

DEVICE

ActiPatch(TM)

Assigned by randomization, this study group will be comprised of subjects that receive the PEMF ActiPatch(TM) treatment for postoperative management of pain and edema.

DEVICE

Placebo

Assigned by randomization, this control group will be comprised of the subjects that receive a placebo patch as treatment for postoperative management of pain and edema.

Trial Locations (1)

02111

Tufts University School of Dental Medicine Department of Oral and Maxillofacial Surgery, Boston