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The effect of hydroalcoholic extract of coriander seed on primary dysmenorrhea

The effect of hydroalcoholic extract of coriander seed on primary dysmenorrhea

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230315057729N1
Enrollment
70
Registered
2023-05-31
Start date
2023-06-10
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

primary dysmenorrhea. Primary dysmenorrhea

Interventions

Intervention 1: Intervention group: 35 girls living in the dormitories of Ferdowsi University, who meet the inclusion criteria, were given oral capsules containing hydroalcoholic extract of coriander

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Be single Be in the age range of 18-30 years Have regular menstrual cycles Have moderate to severe dysmenorrhea Do not have a history of pelvic and abdominal disease Do not have a history of chronic diseases Do not have a history of pain in the abdomen and back except during menstrual bleeding Do not have a history of confirmed mental illnesses Not having severe mental stress in the last 6 months Not allergic to coriander Informed consent to participate in the study

Exclusion criteria

Exclusion criteria: Unwillingness to continue cooperation The occurrence of a severe stressful event during the study period Taking contraceptives Irregular use of medicine or placebo in the amount of two consecutive doses Getting married during the study period Performing professional sports activities Taking any type of supplement and multivitamin Presence of benign breast or uterine cysts They have had a history of prostate cancer, breast cancer and ovarian cancer in their first degree relatives Use of other herbs or drugs effective on dysmenorrhea

Design outcomes

Primary

MeasureTime frame
Intensity and duration of pain in early painful menstruation. Timepoint: Measuring the intensity and duration of painful menstruation at the end of menstrual bleeding during two consecutive cycles and simultaneously with the start of the drug or placebo. Method of measurement: Questionnaires made by the researcher. Visual Analogue Scale.

Secondary

MeasureTime frame
The amount of menstrual bleeding - duration of menstrual bleeding - physical symptoms associated with menstruation. Timepoint: After the end of menstrual bleeding in two consecutive cycles and at the same time as giving medicine or placebo. Method of measurement: Questionnaires made by the researcher.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohre Shahri

Mashhad University of Medical Sciences

shahriz981@mums.ac.ir+98 54 3261 2156

Outcome results

None listed

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