CEFALY Publishes the First and Largest, Phase 3 Clinical Trial of 2-hour External Trigeminal Nerve Stimulation (e-TNS) for At-Home Acute Migraine Treatment
First Real-World, Randomized, Sham-Controlled Clinical Trial of 2-Hour External Trigeminal Nerve Stimulation (e-TNS) in Finds That the e-TNS CEFALY Device Is Effective in Treating Acute Migraine Pain
DARIEN, Conn., April 5, 2022 /PRNewswire/ -- CEFALY Technology, a Belgium-based manufacturer of wearable medical devices for migraine, today announced the results of a clinical study demonstrating that two-hour treatment with the e-TNS CEFALY device is a safe and effective, non-pharmaceutical alternative for the acute treatment of migraine attacks in the out-of-hospital setting.
The Trial of e-TNS for the Acute treatment of Migraine (TEAM) study was the first, prospective, double-blind,randomized, sham-controlled clinical trial of 2-hour e-TNS treatment for acute migraine attack in an at-home scenario. The TEAM study is also the largest sham-controlled, clinical trial examining the use of any e-TNS therapy for the treatment of migraine headache.
A common and debilitating neurological disorder, migraine has been ranked by the World
Health Organization as the world's second leading cause of disability. There are several limitations to conventional anti-migraine medications. In addition, many patients prefer to avoid medications to treat their migraine headaches. As a result, up to 40% of migraine patients have unmet needs for this migraine treatment.
External trigeminal nerve stimulation (e-TNS) is a medical device treatment that offers a non-pharmacological, non-invasive approach for patients with migraine who prefer to avoid medications, have intolerances to medications or, require complementary therapy in their migraine management. Worn on the forehead, the CEFALY e-TNS device delivers a mild electric stimulation to reduce pain signals of the trigeminal nerve, a primary pathway for migraine pain.
The TEAM study spanned nine months and was conducted at 10 centers across the United States. The study enrolled 538 patients aged 18-65 with episodic migraine, with or without aura, who had moderate- to severe-intensity migraine attacks 2 to 8 times per month. Subjects who met all of the study criteria were randomly assigned to either the verum or sham group and were provided a headache diary and educated with how to use the CEFALY device.
During a 2 month period, patients were instructed to self-administer the e-TNS treatment, according to the training and instruction they received, within 4 hours of migraine onset or within 4 hours of awakening with migraine headache. Neurostimulation was applied with the CEFALY e-TNS device for a 2-hour, continuous session.
In the verum group, compared to the sham group:
- Pain freedom at 2 hours was 7.2% higher (25.5% compared to 18.3%; p = .043)
- Resolution of the most bothersome migraine-associated symptom was 14.1% higher (56.4% compared to 42.3%; p = 0.001)
- Pain relief at 2 hours was 14.3% higher (69.5% compared to 55.2%; p = 0.001)
- Absence of all migraine-associated symptoms at 2 hours was 8.4% higher (42.5% compared to 34.1%; p = 0.044)
- Sustained pain freedom and pain relief at 24 hours was 7.0% and 11.5% higher in verum (22.8% and 45.9%) than sham (15.8 and 34.4%; p = 0.039)
No serious adverse events were reported.
Study authors concluded that the use of self-administered 2-hour e-TNS therapy is a safe and effective therapeutic option, with or without the use of acute anti-migraine medications.
"The CEFALY device provides patients with a non-medication option for the prevention and acute treatment of migraine. It is especially helpful to add to a medication regimen or use for people who have had a negative experience with migraine medications," said Dr. Deena Kuruvilla, one of the study authors and Medical Director and Board Certified Neurologist, Westport Headache Institute.
"So many people who live with migraine pain are desperate for a solution that they can use safely at home," said Jen Trainor McDermott, CEO of CEFALY Technology. "As the TEAM study shows us, CEFALY provides the powerful, sustained pain relief they need."
About the CEFALY device:
CEFALY Technology is the maker of the CEFALY DUAL Enhanced, the FDA-cleared, over-the-counter wearable medical device clinically proven to help reduce migraine frequency and relieve migraine pain. CEFALY DUAL Enhanced is a non-invasive device placed on the forehead to modify pain sensation in the area research identifies as a center for migraine pain, the trigeminal nerve. The device offers two distinct treatment options -— a 60-minute ACUTE setting that serves as an abortive treatment for pain relief at the onset of a migraine, which is clinically proven to stop or reduce migraine pain during an attack; and a 20-minute PREVENT setting for daily use to help prevent future episodes.
About CEFALY Technology:
CEFALY Technology is a Belgium based company with U.S. offices based in Darien, Conn., specializing in electronics for medical applications. CEFALY Technology's mission is to provide the migraine community with forward-thinking treatments that are drug-free and clinically-proven to relieve and prevent future attacks.
Learn more about CEFALY by visiting www.CEFALY.com and following us on Facebook, Twitter, LinkedIn and Instagram.
Media Contact:
Jen Trainor McDermott
CEO Cefaly Technology
[email protected]
Mobile 516-456-4110
SOURCE Cefaly Technology
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