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Effect of geranium on dysmenorrhea

The effect of massage with geranium essence on pain severity of primary dysmenorrhea

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017013132329N1
Enrollment
90
Registered
2017-04-06
Start date
2017-04-04
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: In the control group no intervention will be done by researcher and Only subject's pain intensity will be measured. Intervention 2: In intervention group geranium essence 5%manufactur
Placebo
In the control group no intervention will be done by researcher and Only subject's pain intensity will be measured.
In second group of odorless almond oil manufacturing by barij essence company will be used.In this group with 20 cc of almond oil massage to form of circular in the upper part of the pubic done for 15
In intervention group geranium essence 5%manufacturing by barij essence company will be used.Geranium essence in odorless sweet almond oils as the base oil is diluted.in intervention group essence c

Sponsors

Gonabad University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:being single;Age 35-18 years; having regular menstruation periods intervals of 35-21 day; accordingto the Visual Analogue Scale score higher than 5; The lack of a history of physical diseases:such as asthma; allergies; migraines; diabetes; thalassemia;blood pressure; thyroid disease; cardiovascular and lack of pelvic inflammatory disease;uterine and ovarian cyst diagnosed as abnormal bleeding; the lack of hormone therapy and oral contraceptive pills during the last 3 months.Exclusion criteria: Not wanting to continue participating in the study;occurence abnormal bleeding during the study;use of analgesics during the stud; indicated any allergic reaction to essential oils.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain of dysmenorrhea. Timepoint: Before, immediately after and 24 hours after intervention. Method of measurement: visual anaoge scale.

Secondary

MeasureTime frame
Side effects. Timepoint: In the period cycle after intervention. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahanaz Abavisani

Gonabad University of Medical Science

m.abavisani@gmu.ac.irmahnazabavisani@gmail.com+98 51 5722 3028

Outcome results

None listed

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