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17 • Space closure of extraction site to be performed on stainless steel wire of dimensions ≥ 0.018” OR ≥ 0.016’ x 0.022” Exclusion criteria: • Presence of systemic illnesses • Current exposure to medicines • Pregnancy • Previous orthodontic therapy • Smokers Potential participants (and parents and guardians) were verbally informed of the study rationale and design. In addition, they were provided with written documents detailing information that included the following: privacy and security policies for use of their personal information in the study, a description of the LED device, a user manual for the LED device, documentation illustrating the safety of the LED device and an overview of the study validity, rationale and protocol (see Appendix A). Patients were then given the opportunity to review the documents at their leisure and had all questions answered prior to consenting to participate in the study. Following informed consent, all potentially participating patients were monitored until extraction space closure was to be actively undertaken. If the extraction spaces were viewed as being fairly symmetric and of adequate size (see inclusion criteria above) they were included in the study. These patient recruitment parameters yielded 37 potential study participants of which 11 patients were finally included in the study.PDF Image | Effect of LED Phototherapy on the Rate of Orthodontic Tooth Movement
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