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Effect of oral Royal jelly on severity of premenstrual syndrome

Phase 1
Conditions
Premenstrual syndrome.
Premenstrual tension syndrome
Registration Number
IRCT201107192172N12
Lead Sponsor
Vice chancellor for research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
110
Inclusion Criteria

age between 20 and 35 years old; not taking any medicine; having symptoms in 2 past cycles; not taking any complements; no allergy to honey or Royal jelly; no changes in diet & exercise program; not smoking, alcohol or drug usage
Exclusion criteria: use of any kind of drug or therapy for symptom relief during the study intervention; side effects during intervention for example allergy; change in diet or physical exercise program during the study; any kind of crisis in participant or her family; not taking royale jelly or placebo more than 7 days in 2 cycles

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Premenstrual syndrome (screening). Timepoint: 2 menstrual cycles. Method of measurement: premenstural profile 2005 scale.
Secondary Outcome Measures
NameTimeMethod
Premenstrual syndrome (prevention). Timepoint: during intervention for 2 cycles. Method of measurement: premenstrual profile 2005 scale.
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