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Comparing the effect of topical ginger oil with oral ginger on primary dysmenorrhea

Comparing the effect of topical ginger oil with oral ginger on primary dysmenorrhea

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014090219012N1
Enrollment
34
Registered
2015-05-16
Start date
2014-09-23
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

primary dysmenorrhea. primary dysmenorrha

Interventions

Intervention 1: 250 mg capsule of ginger every 6 hours from two days before the onset of the menstrual period until the first three days of the menstrual period for 3 consequent cycles. Intervention 2
Treatment - Drugs
250 mg capsule of ginger every 6 hours from two days before the onset of the menstrual period until the first three days of the menstrual period for 3 consequent cycles
Ointment 5 drops ginger oil on the abdomen under umbilicus every 6 hours, from two days before the onset of the menstrual period until the first three days of the menstrual period for 3 consequent cyc

Sponsors

School of Traditional Medicine, Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 18-45 years; BMI = 35; regular menstrual cycles (21-35day) and Regular bleeding (3-10days) in the latest three menses; moderate and severe dysmenorrhea (grade 2,3) based on Multidimensional Verbal Scoring System; rejection of Secondary dysmenorrhea by history and pelvic ultrasound; no History of pelvic or abdominal surgery; not taking other medications; no history of allergy to ginger; no history of bleeding disease; no history of gallstone. Exclusion Criteria: pregnancy; sensitivity to medication during the study; avoiding the correct use of medication; taking another drug that is not defined in the study; patients with Possible serious side effects; patients who need additional interventions and surgery; patients who decide to be excluded.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: cycle before intervention, every cycles during intervention (3 cycles). Method of measurement: VAS = visual analog scale.;Pain duration. Timepoint: cycle before intervention, every cycles during intervention (3 cycles). Method of measurement: hour.

Secondary

MeasureTime frame
Side effect: Stomachache, nasea, vomiting, hematemesis, belch, fatigue, itching, acne, heartburn, diarrhea, constipation, melena,headache, drowsiness, redness, assessment of bleeding with PBAC. Timepoint: cycle before intervention, every cycle during intervention (3 cycles). Method of measurement: questionnaire.;Mefenamic asid use. Timepoint: cycle before intervention, every cycle during intervention (3 cycles). Method of measurement: number.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPantea Shirooye

School of Traditional Medicine, Shahid Beheshti University of Medical Sciences

http://traditional.sbmu.ac.ir+98 21 8877 3521

Outcome results

None listed

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