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The primary outcome was pain, specifically a reduction in pain (i.e., menstrual pain) that occurred only during the intervention or as a result of the intervention measured by a visual analogue scale (VAS), by other validated scales, or as a dichotomous outcome. The secondary outcome was AEs.
Copyright and License information: ©2018 by the authors.
Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
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