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The effect of zataria-multiflora on premenstrual syndrome severity

The effect of zataria-multiflora on premenstrual syndrome severity in the students of Isfahan University of Medical Sciences 1391-1392.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012102211212N1
Enrollment
120
Registered
2012-12-24
Start date
2012-10-19
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

Premenstrual syndrome. Premenstrual tension syndrome

Interventions

Intervention 1: Control group: placebo capsules 2 times a day (2 tablets every 12 hours) for 7 days prior to the first day of the menstrual cycle. Intervention 2: Soft capsules containing 20 mg of ess
Treatment - Drugs
Control group: placebo capsules 2 times a day (2 tablets every 12 hours) for 7 days prior to the first day of the menstrual cycle
Soft capsules containing 20 mg of essential oil and 2 times a day (every 12 hours 2 tablets) for 7 days prior to the first day of the menstrual cycle

Sponsors

Vice chancellor for research, Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age range of 18-35 years; a mark of at least 5 of the questionnaire to detect symptoms of temporary Pms; that at least one of the five symptoms of psychiatric symptoms and the severity of each offense included within the average or more during the past two months ; having a regular menstrual cycle; lack of stressor during the previous 3 months; lack of physical illness and mental; Non-hormonal medications and anti depressants. Exclusion criteria: Persons who during the study Getting sick; being hospitalized;being pregnant; the reading experience of be stressful; those who do not use the medicine properly; or do not complete the form correctly.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The severity of premenstrual syndrome. Timepoint: 2 months before the study, 2 months after the intervention. Method of measurement: Daily chart position.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Sodouri

Kashan University of Medical Sciences

Alavi.negin@yahoo.com;marziehsodouri@yahoo.com;sodouri@kaums.ac.ir+98 36 1555 2999

Outcome results

None listed

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