Primary Dysmenorreh pain severity

Not Applicable

• Conditions: Primary Dysmenorreh.; Pain and other conditions associated with female genital organs and menstrual cycle

• Registration Number: IRCT2015031521475N1
• Lead Sponsor: Vice chancellor for reserch of Kermanshah University Of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 42

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

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.