Survey on Menstrual Symptoms, Health Related Quality of Life and Work Productivity in Patients Suffering From Pain During Menstruation (Dysmenorrhea) in Japan

Dysmenorrhea Clinical Trial

Official title:

Patient Panel Survey on Menstrual Symptoms, HRQoL and Work Productivity in Patients With Primary or Secondary Dysmenorrhea in Japan

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04607382
• Other study ID #: 21420
• Status: Completed
• Start date: September 23, 2020
• Est. completion date: June 30, 2021

Study information

• Verified date: June 2022
• Source: Bayer
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

In this study researcher want to gain more information on the treatment effect of Low-dose Estrogen Progestin (a hormone treatment) on the health related quality of life and work productivity in patients suffering from menstrual pain. The treating doctors will ask the study participants to complete questionnaires at start of study, after 2 and 4 months (end of study). The questions will be about participant's general and mental health, concentration, behavioral and emotional changes, and work productivity and activity level. This study will be conducted in Japan and enrols about 380 female participants in the age range of 16 to 39 years.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 397
• Est. completion date: June 30, 2021
• Est. primary completion date: June 30, 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 16 Years to 39 Years

Eligibility

Female patients with a diagnosis of dysmenorrhea will be enrolled after the decision for treatment with LEP or Non-LEP has been made by the physician. Patients who have been prescribed LEP or Non-LEP for a medically appropriate use will be eligible to be enrolled. Indications and contraindications according to the local market authorization should be carefully considered. Evidence of assessment of all eligibility criteria by the patients, as well as enrollment of a patient in the study should be documented in database of M3.

Inclusion Criteria:

Patients who meet all the inclusion criteria will be enrolled in this study.

• Patients between the ages of 16 and 39

• Patients diagnosed with primary or secondary dysmenorrhea by gynecologists

• Patients who can visit ob/gyn clinics or hospitals every 6 months to have consultations with gynecologists for treatment of dysmenorrhea

• Patients who plan to be treated with drug for dysmenorrhea after enrollment in this study

• Patients who are currently on Non-LEP therapies will be eligible for LEP cohort**

• Patients who can access the website to complete the questionnaire using mobile communication equipment such as mobile phones or tablets

• Patients who submit an informed consent on the website before the start of this study

Exclusion Criteria:

Patients who meet any of the exclusion criteria will not be enrolled in this study.

• Patients who have taken LEP for dysmenorrhea in the last 2 months before enrollment*

• Patients with mental disorders such as depression, severe infectious diseases, or malignant tumors

• Patients who do not meet the inclusion criteria.

Patients with contraindications for LEP or COC are as follows:

• Women who have a predisposition to hypersensitivity to the ingredients of this product

• Breast cancer patients

• Patients with undiagnosed abnormal genital bleeding

• Patients with thrombophlebitis, pulmonary embolism, cerebrovascular disease, coronary artery disease, or a history of the same

• Smokers over the age of 35 who smoke more than 15 cigarettes a day

• Patients with migraine with antecedents (flashing lights, star-shaped flashes, etc.)

• Patients with valvular heart disease complicated by pulmonary hypertension or atrial fibrillation and with a history of subacute bacterial endocarditis

• Diabetic patients with vascular lesions (diabetic nephropathy, diabetic retinopathy, etc.)

• Patients with thrombotic predisposition

• Patients with antiphospholipid antibody syndrome

• Patients with major surgeries of 30 minutes or more, within 4 weeks before surgery, within 2 weeks after surgery, and in patients with long-term rest

• Patients with severe liver damage.

• Patients with liver tumors

• Hypertension (except for patients with mild hypertension)

• Otosclerosis

• Patients with a history of jaundice, persistent pruritus, or herpes pregnancy during pregnancy

• Women who are pregnant or who may be pregnant

• Breastfeeding women under 6 months of age

• Patients taking contraindicated drugs for LEP or COC

Related Conditions & MeSH terms

• Dysmenorrhea

Intervention

Drug:
• LEP
LEP dosage up to the discretion of the treating gynecologists.
• NSAIDs and/or Chinese medicine (CM)
Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) and Chinese medicine (CM) dosage up to the discretion of the treating gynecologists.

Locations

Country	Name	City	State
Japan	Multiple Facilities	Multiple Locations

Sponsors (1)

Lead Sponsor	Collaborator
Bayer

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in Menstrual Distress: evaluated by modified Menstrual Distress Questionnaire (mMDQ)	To describe the changes in menstrual symptoms before, during and after the study in Low-dose Estrogen Progestin product (LEP) cohort.	Baseline, 60 days and 120 days
Primary	Changes in Health Related Quality of Life (HRQoL): evaluated by Short Form (36) Health Survey version 2 (SF-36v2)	To describe the changes in HRQoL before, during and after the study in LEP cohort.; The SF-36v2 will be assessed on a 3- and 5-point Likert scale. The rating scale depends on each question.	Baseline, 60 days and 120 days
Primary	Changes in work productivity (mWPAI)	To describe the changes in work productivity before, during and after the study in LEP cohort.	Baseline, 60 days and 120 days
Primary	Changes in Activity Impairment: evaluated by General Health v2.0 (WPAI-GH)	To describe the changes in activity impairment before, during and after the study in LEP cohort.	Baseline, 60 days and 120 days
Secondary	Description of patients' background and medical history of LEP and Non-LEP cohorts	To describe patients' background and medical history of LEP and Non-LEP cohorts	Baseline
Secondary	Change in mMDQ of Non-LEP cohort	To describe the change in menstrual symptoms before, during and after the study in Non-LEP cohort.	Baseline, 60 days and 120 days
Secondary	Change in HRQoL of Non-LEP cohort	To describe the change in HRQoL before, during and after the study in Non-LEP cohort.	Baseline, 60 days and 120 days
Secondary	Change in work productivity of Non-LEP cohort	To describe the change in work productivity before, during and after the study in Non-LEP cohort.	Baseline, 60 days and 120 days