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Clinical Trials/JPRN-UMIN000041802
JPRN-UMIN000041802
Completed
未知

A prospective observational study on menstrual symptoms, HRQoL, and work productivity in patients with primary or secondary dysmenorrhea before, during, and after treatment with LEP or non-LEP in Japan - A prospective observational study on menstrual symptoms, HRQoL, and work productivity in patients with primary or secondary dysmenorrhea before, during, and after treatment with LEP or non-LEP in Japan

Bayer Yakuhin, Ltd.0 sites495 target enrollmentSeptember 15, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Primary and secondary dysmenorrhea
Sponsor
Bayer Yakuhin, Ltd.
Enrollment
495
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 15, 2020
End Date
November 30, 2020
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Patients who meet any of the exclusion criteria will not be enrolled in this study. 1\) Patients who have taken LEP for dysmenorrhea in the last 2 months before enrollment 2\) Patients with mental disorders such as depression, severe infectious diseases, or malignant tumors 3\) Patients with contraindications for LEP or COC 4\) Patients who deemed by the investigators to be unsuitable for inclusion in the study (e.g., patients using hormonal agents other than LEP)

Outcomes

Primary Outcomes

Not specified

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