MINNEAPOLIS--(BUSINESS WIRE)--Dec. 9, 2011-- Clinical trial data presented at the 15th Annual Meeting of the North American Neuromodulation Society demonstrate the AdaptiveStim™ with...
AdaptiveStim with RestoreSensor, approved by the
At the end of the study, 86.5 percent of study participants with chronic pain, who were included in an intent-to-treat analysis (n=74), experienced somewhat better or much better pain relief with no loss of convenience, or somewhat more or much more convenience with no loss of pain relief, when the device’s AdaptiveStim technology was turned on, compared to a control period when the participants manually adjusted neurostimulation settings using a patient programmer.
With AdaptiveStim, study participants also reported functional improvements, including improved comfort during position changes (80.3 percent). When the study ended, 90.1 percent of the participants said they intended to use AdaptiveStim, either by leaving it on all or most of the time or by turning it on or off as needed.
Additionally, when AdaptiveStim was turned on, a 41 percent reduction in the average number of manual programming changes needed to adjust stimulation throughout the day was noted. Physicians reported a clinical benefit for 88.7 percent of participants with AdaptiveStim.
The multicenter, prospective, open-label, randomized, crossover study enrolled 79 study participants at 10 U.S. centers. Seventy-six participants received implants and were randomized to receive either stimulation from the RestoreSensor device for six weeks with the AdaptiveStim technology turned on followed by six weeks with AdaptiveStim turned off, or six weeks with AdaptiveStim turned off followed by six weeks with AdaptiveStim turned on. When AdaptiveStim was turned off, participants manually adjusted stimulation levels using a patient programmer.
“This study clearly demonstrates the effectiveness of position-adaptive stimulation technology in providing pain relief and convenience to patients suffering from chronic pain, so they can lead more normal lives,” said
The profile of adverse events reported during the U.S. clinical trial was similar with and without the AdaptiveStim technology activated.
Worldwide, nearly 200,000 people have received
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