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The effect of Fennel on treatment Dysmenorrhea

Comparison of the effect of Fennel and Gelofen on the severity of primary Menstrual pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016060728313N1
Enrollment
72
Registered
2016-08-12
Start date
2016-06-09
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 Dysmenorrhoea

Interventions

Intervention 1: Medicine and registration form (for before and after the use of medicine) for the first cycle will be distributed and information on how to take the medicine is presented to everybody
Treatment - Other
Treatment - Drugs
Medicine and registration form (for before and after the use of medicine) for the first cycle will be distributed and information on how to take the medicine is presented to everybody in Experimental
Medicine and registration form (for before and after the use of medicine) for the first cycle will be distributed and information on how to take the medicine is presented to everybody in Control Grou

Sponsors

Islamic Azad University Of Ardabil Branch
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The incidence of primary dysmenorrhea grade 2 and 3 according to verbal multidimensional scoring criteria. Exclusion criteria: Use of birth control pills and herbal medicines; As well as painkillers and other relaxation techniques or acupressure to relieve dysmenorrhea; Having of renal; hepatic; respiratory; and blood diseases; Having of sensitivity to NSAIDs and fennel.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The severity of Menstrual pain. Timepoint: Three months after the begining of interaction. Method of measurement: Verbal Multidimensional Scoring Criteria.

Secondary

MeasureTime frame
Side Effects. Timepoint: Three months after the begining of interaction. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoya Motavalli

Islamic Azad University Of Ardabil Branch

mrmotavalli@yahoo.com+98 45 3372 8025

Outcome results

None listed

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