The new FDA-approval follows several clinical trials that demonstrated that one hour of e-TNS with the Cefaly ACUTE can relieve or stop the migraine headache.
Renowned for helping prevent migraine attacks, a new FDA clearance paves way for more Cefaly devices that can now stop a migraine in progress and prevent a future episode too |
| [29-November-2017] |
| NEW YORK, Nov. 29, 2017 /PRNewswire/ -- Cefaly announces today the release of two new U.S. Food and Drug Administration (FDA)-approved migraine treatment devices. Cefaly®, already the first FDA-approved external trigeminal nerve stimulation (e-TNS) device for the prevention of migraine attacks, is now the only migraine device available for use during a migraine attack with or without aura. The Cefaly® ACUTE can help rescue a migraine already in progress. The Cefaly® DUAL is a device that combines the newly approved ACUTE treatment with its prophylactic predecessor, the Cefaly® 2; now more appropriately renamed Cefaly® PREVENT. “We are excited that we can now offer migraine patients several drug-free options in their migraine care,” said Dr. Pierre Rigaux, the chief executive officer of CEFALY Technology, and a member of the team that invented the device. “We have developed a way for migraine patients to stop a migraine and prevent a migraine without medication and with next-to-no side effects.” The new FDA-approval follows several clinical trials that demonstrated that one hour of e-TNS with the Cefaly® ACUTE can relieve or stop the migraine headache. Results from the acute treatment of migraine with external trigeminal nerve stimulation double-blind randomized placebo control trial were presented at a recent meeting of the International Headache Society. The findings showed that on average, the Cefaly® treatment reduced migraine pain by 65%. In addition, 32% of patients were pain free within an hour. Proprietary Cefaly® technology has been adapted to efficiently and safely address the different phases of migraines. There are now three treatment options: Cefaly® PREVENT, a prophylaxis treatment; Cefaly® ACUTE, a rescue treatment, and Cefaly® DUAL, a device that combines both prevent and acute technologies. Despite these differences, the devices are administered in the same way: a device is placed on the forehead via a magnetic connection to a self-adhesive electrode, which then sends precise micro-impulses through the skin to the upper branches of the trigeminal nerve to either relieve headache pain during a migraine attack or to prevent a future migraine attack. All Cefaly® devices are available to adults by prescription-only. About CEFALY Technology Media Contact: Maria Coder View original content:http://www.prnewswire.com/news-releases/fda-approved-cefaly-device-to-stop-migraines-now-available-300563323.html SOURCE CEFALY Technology |
