About this trial
This study will assess the effects of the rose tablet candies produced by MRJPs on the subjects, evaluate the role of MRJPs in the ovarian function and endometrial receptivity of women, reveal the potential application value of MRJPs in reproductive health, and determine its safety and effectiveness.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Fertile women, aged 20 to 45 years old, with regular and normal menstrual cycles.
Disqualifiers
① Allergic to royal jelly or its components; ② Suffering from severe chronic diseases or endocrine system disorders; ③ Pregnant or breastfeeding; ④ Undergoing hormone replacement therapy (HRT) within the last month
Trial design
Parallel
Treatments tested in this trial
Oral MRJPs Candy
Dietary supplement500 mg per tablet, containing 70% MRJPs freeze-dried powder + 20% sodium cellulose + 10% microcrystalline cellulose, with an appropriate amount of arabinose, taken twice a day, 1 tablet each time, for a total of 1 menstrual cycle in the control group.
Oral placebo candy
Dietary supplement500 mg per tablet, containing 70% whey protein powder + 20% sodium cellulose + 10% microcrystalline cellulose, with appropriate amount of arabinose, taken twice a day, 1 tablet each time, for a total of 1 menstrual cycle in the control group.
Treatment groups
Trial outcomes
Primary outcomes
Anti-Müllerian hormone
Ovarian function testing indicator
Secondary outcomes
Sex hormone levels
Basic follicle-stimulating hormone
Endometrial receptivity
Ultrasound examination during the luteal phase to assess endometrial receptivity
Sex hormone levels
Basic luteinizing hormone
Sex hormone levels
Basal estradiol hormone
Sponsors and contacts
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