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A randomized, controlled, crossover study of the Good Morning Snore Solution by MPowRx for sleep disordered breathing was conducted by Calgary dental researcher, Dr. Leslie Dort (MSc, DDS, Dip ABDSM) and published in the Journal of Sleep and Breathing, May 2008.

A group of 32 patients were subjected to randomized, controlled cross-over study involving the anti-snoring mouthpiece - Good Morning Snore Solution by MPowRx and a control device of a similar design but without the suction mechanism.

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Patients used each device for one week, and were evaluated according to three standard industry measures of snoring: The Respiratory Disturbance Index (RDI), a measure of the number of sleep disturbances divided by the number of hours sleep; the Snoring Index, which measures the average number of snores per hour; and Epworth Sleepiness Scale (ESS), a measure of sleep propensity during the day as perceived by the subjects and derived from the answers to eight questions.

All subjects had to have a primary diagnosis of snoring by a physician to participate in the study. The results of the study are summarized below:

On average, RDI was reduced by at least 50% in 34% of subjects, resulting in a clinically significant reduction in the number of disturbances to less than 10 per hour. The definition of therapeutic success is a reduction in RDI to <10 per hour. Four out of five subjects with severe OSA (RDI>30), showed reduction in RDI of at least 50%.
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