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Ginger capsule and frankincense effect on uterine hemorrhage

Clinical trial of comparison between frankincense (Boswellia serrata) capsule and ginger (Zingiber officinale) capsule on reducing heavy menstrual bleeding among women at the age of 18-45 years

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016062228579N1
Enrollment
90
Registered
2017-02-03
Start date
2016-08-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heavy menstrual bleeding. Excessive and frequent menstruation with regular cycle

Interventions

Intervention 1: Intervention group 1: Frankincense capsule and ibuprofen tablet will be prescribed for the patients, three times a day, from first to the last day of menstrual period. This order will
Treatment - Drugs
Placebo
Intervention group 1: Frankincense capsule and ibuprofen tablet will be prescribed for the patients, three times a day, from first to the last day of menstrual period. This order will be followed in t
Intervention group 2: Ginger capsule and ibuprofen tablet will be prescribed for the patients, three times a day, from first to the last day of menstrual period. This order will be followed in two con
Control group: Placebo capsule and ibuprofen tablet will be prescribed for the patients, three times a day, from first to the last day of menstrual period. This order will be followed in two consecuti

Sponsors

Vice chacellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Outpatient women at the age of 18-45years; Regular 22- 35 day menstrual cycles; presence of menorrhagia based on Higham bleeding assessment chart (bleeding more than 80 ml per cycle, or more than 7 days); absence of moderate or severe anemia (hemoglobin greater than 10.5 milligrams per deciliter); The absence of uterine fibroma or being smaller than 5 cm; The absence of ovarian cysts; Not using hormonal drugs or any medication affecting menstrual bleeding (oral contraceptive pills and aspirin, warfarin); normal endometrial thickness in abdominal or trans vaginal ultrasound; The patient is not pregnant or during lactation. Exclusion criteria: pregnancy; breast feeding; taking hormonal drugs or mefenamic acid during their menstruation period; being allergic to ginger or frankincense; severe bleeding during menstruation period requiring emergency measures.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menstrual blood volume. Timepoint: The end of each menstrual cycle. Method of measurement: Pictorial Blood Loss Assessment (PBAC).;Time period (days) of menstrual bleeding. Timepoint: The end of each menstrual cycle. Method of measurement: Pictorial Blood Loss Assessment (PBAC).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh Eshaghian

Isfahan University of Medical Sciences

r_eshaghian@resident.mui.ac.ir+98 31 3376 7525

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026