A Randomized Controlled Study on the Effect of MRJPs on Improving Ovarian Function and Endometrial Receptivity

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-45
SponsorThe Fourth Affiliated Hospital of Zhejiang University School of Medicine

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Oral MRJPs Candy

    Dietary supplement

    500 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 supplement

    500 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

66 Participants
are divided into 2 treatment groups
Group A: Experimental groupExperimental treatment 1 intervention
Group B: Control groupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Anti-Müllerian hormone

Ovarian function testing indicator

Time frame
From enrollment to the end of treatment at 1 month

Secondary outcomes

1

Sex hormone levels

Basic follicle-stimulating hormone

Time frame
From enrollment to the end of treatment at 1 month
2

Endometrial receptivity

Ultrasound examination during the luteal phase to assess endometrial receptivity

Time frame
From enrollment to the end of treatment at 1 month
3

Sex hormone levels

Basic luteinizing hormone

Time frame
From enrollment to the end of treatment at 1 month
4

Sex hormone levels

Basal estradiol hormone

Time frame
From enrollment to the end of treatment at 1 month

Other outcomes

Sponsors and contacts

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