Drug Use Investigation (DUI) of YazFlex for Endometriosis-associated Pelvic Pain and/or Dysmenorrhea
Study Details
Study Description
Brief Summary
This study is a Japanese post-marketing surveillance (PMS) which is required by the regulatory authorities. General objective of PMS is to confirm the clinical usefulness, especially the safety profile of a drug under the routine clinical practice.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
Detailed Description
It is a local, non-interventional, multi-center, single-cohort study using primary data of patients treated with YazFlex in endometriosis or dysmenorrhea indication.
A total of 600 patients (300 for endometriosis and 300 for dysmenorrhea) is planned to be enrolled in 2 years.
The treatment should be performed in Japan based on the product label. The patients will be observed for up to 2 years (1 year at the earliest) during their YazFlex treatment.
The outcome variables for the primary objective are treatment emergent adverse events (TEAEs) and adverse drug reactions (ADRs). The outcome variables for the secondary objective include newly developed haemorrhagic ovarian cyst, genital bleeding, severity of dysmenorrhea, pelvic pain and compliance status in the new flexible regimen.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| BAY86-5300_YAZ-Flex Patients with endometriosis-associated pelvic pain or dysmenorrhea |
Drug: BAY86-5300_YAZ-Flex
Patients with endometriosis-associated pelvic pain and/or dysmenorrhea are enrolled solely after the physician's decision of YazFlex treatment in routine clinical practice.
|
Outcome Measures
Primary Outcome Measures
- Number of treatment emergent adverse events (TEAEs) and adverse drug reactions (ADRs) [Up to 2 years ( 1 year at the earliest)]
Events will be summarized by frequency tables (e.g. absolute and relative frequencies) using the MedDRA cording system.
Secondary Outcome Measures
- Change in periodic blood loss [Up to 2 years ( 1 year at the earliest)]
The data incidence proportions of periodic blood loss will be analyzed as course (and change from baseline) during the study with suitable time windows.
- Change from baseline of compliance status in the new flexible regimen [Up to 2 years ( 1 year at the earliest)]
Date of intake
- Days of menorrhagia [Up to 2 years ( 1 year at the earliest)]
Menstrual pain is continuous menstrual pain or lower abdominal pain that is observed for menstruation or withdrawal blood events and may spread to the back or thigh. Pain may be recognized 2 days before bleeding, and ends by the last day of menstruation or withdrawal.
- Number of date of using analgesic [Up to 2 years ( 1 year at the earliest)]
Record the date of using the analgesic.
- Change in severity of pelvic pain by using Numeric Rating Scale (NRS) [Up to 2 years ( 1 year at the earliest)]
The degree of pelvic pain in each menstrual period, menstrual period, sexual intercourse and defecation will be evaluated using NRS score (11 levels from no pain is "0" to highest pain "10" ) in each month.
- Change in severity of dysmenorrhea [Up to 2 years ( 1 year at the earliest)]
The severity will be evaluated and recorded the following criteria. None Somewhat obstructing work (school or housework) get a problem with one's work (studies / housework) because the more one wants to lie down Fall asleep for more than 1 day, and cannot do one's work (school or housework)
- Change in quality of Life by using EQ-5D-5L , EIS and/or MDQ [Up to 2 years ( 1 year at the earliest)]
Endometriosis Impact Scale (EIS) (for disease burden of endometriosis) Menstrual Distress Questionnaire (MDQ) (for disease burden of dysmenorrhea) EQ-5D (for general QOL measurement)
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patients with endometriosis-associated pelvic pain and/or dysmenorrhea.
-
Patients for whom the decision to initiate treatment with YazFlex is made as per physician's clinical practice.
Exclusion Criteria:
- Patients participating in an investigational program with interventions outside of routine clinical practice.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Many locations | Multiple Locations | Japan |
Sponsors and Collaborators
- Bayer
Investigators
- Study Director: Bayer Study Director, Bayer
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 18703