Effect of Bioptron on Primary Dysmenorrhea: a Randomized Controlled Trial
Effect of Bioptron on Primary Dysmenorrhea: a Randomized Controlled Trial
This study will be conducted to determine the effect of bioptron on PD through the assessment of serum progesterone level, and pain level measured by pressure algometry in addition to evaluation of the symptoms of PD and its effect on girl's quality of life through valid and reliable questionnaires which will be of valuable benefits in the women's health fields.
All females will be randomly divided into two equal groups:
Group A (control group):
lt will include 28 participants suffering from PD taking vitamin D (vitamin D) supplements for three consecutive menstrual cycles.
Group B (study group):
lt will include 28 participants suffering from PD who will take vitamin D (vitamin D) supplementations as in group A in addition to Bioptron for 20 min daily for 7 days before the menstrual cycle along with the first three days of menstrual flow for three consecutive menstrual cycles.
All females will be given a full explanation of the study protocol and a consent form will be signed by each female before entry in the study
Inclusion Criteria:
All females will be clinically diagnosed by the gynecologist with primary dysmenorrhea.
B) Exclusion Criteria:
Participants will be excluded if they have:
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