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Primary Dysmenorreh pain severity

The study of the effects of Melatonin and Meloxicam on sleep quality and pain severity in patients with primary dysmenorreh

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015031521475N1
Enrollment
42
Registered
2015-07-10
Start date
2015-06-22
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 Dysmenorreh. Pain and other conditions associated with female genital organs and menstrual cycle

Interventions

Intervention 1: Control group : Folic Acid 10 mg with Folate brand name of pharmaceutical manufacturer Mehr, Once at night for 5 night in the menstrual cycles before intervention and time intervention
Placebo
Treatment - Drugs
Control group : Folic Acid 10 mg with Folate brand name of pharmaceutical manufacturer Mehr, Once at night for 5 night in the menstrual cycles before intervention and time intervention
Intervention group 1 : Melatonin 3 mg of pharmaceutical manufacturer seppid drug, Once at night for 5 night in the menstrual cycles before intervention and time intervention, Chemical combination acet
Intervention group 2 : Meloxicam 7.5 mg of Manufacturer compani Loghman with mubik brand name, Once at night for 5 night, in the menstrual cycles before intervention and time intervention

Sponsors

Vice chancellor for reserch of Kermanshah University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Women 18 to 35 years old and nulipar; Regular cycles 21 to 35 days; Normal BMI 19.8 to 25; Medicines and certain supplements and herbal medicines not used in before and during of the study, Exclusion criteria: Secondary dysmenorrhea from pelvic disorders; Chronic diseases; Mental disorders; Lack of person satisfaction in order to participating continue in the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Dysmenorreh Pain Severity. Timepoint: The menstrual cycle before intervention and during intervention for 5 night. Method of measurement: According to the Mac Gill pain scale ruler.;Quality Of Sleep. Timepoint: The menstrual cycle before intervention and during intervention for 5 night. Method of measurement: According to the results Acti graphic.

Secondary

MeasureTime frame
BMI. Timepoint: The menstrual cycle before intervention and during intervention for 5 night. Method of measurement: The result of dividing weight on the square of height.;Bed Time. Timepoint: The menstrual cycle before intervention and during intervention for 5 night. Method of measurement: According to the results Acti graphic.;The Duration Of Sleep. Timepoint: The menstrual cycle before intervention and during intervention for 5 night. Method of measurement: According to the results Acti graphic.;Waking At Night. Timepoint: The menstrual cycle before intervention and during intervention for 5 night. Method of measurement: According to the results Acti graphic.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Farahnaz Keshavarzi

Kermanshah University of Medical Sciences

Farahnaz Keshavarzi @yahoo.com+98 83 3427 6331

Outcome results

None listed

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