Overview
Mirena in Idiopathic Menorrhagia
Status:
Completed
Completed
Trial end date:
2008-11-01
2008-11-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
This is an open-label, uncontrolled, multi-centre observational study that analyses a follow-up of 1600 women with dysfunctional uterine bleeding (idiopathic menorrhagia) over a period of one year.The patients evaluated at four visits, beginning with the insertion visit and 3, 6 and 12 months after insertion.Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
BayerTreatments:
Levonorgestrel
Criteria
Inclusion Criteria:- Woman diagnosed with idiopathic Menorrhagia according to assessment of the
investigator and according to international guidelines. These woman should also accept
to be on contraception during the time period that they have Mirena in situ.
- Age limit 30-45
- BMI= 18-34
- Signed informed consent
Exclusion Criteria:
- Medical conditions featured in the Mirena data sheet (See Appendix 1) that
contraindicate its use, listed below:
- Known or suspected pregnancy; current or recurrent pelvic inflammatory disease;
infection of the lower genital tract; postpartum endometritis; septic abortion during
the past three months; cervicitis; cervical dysplasia; uterine or cervical malignancy;
undiagnosed abnormal uterine bleeding; congenital or acquired abnormality of the
uterus including fibroids if they distort the uterine cavity; conditions associated
with increased susceptibility to infections; acute liver disease or liver tumor; known
hypersensitivity to any of the constituents of the product.
- Nulliparity
- Consumption of Iron, Antiprostaglandins, hormonal drugs and any medication that could
effect bleeding should be stopped at least 3 months before the first visit and should
not be used during the course of the study.
- History of diabetes mellitus,cardiovascular disease and thyroid abnormalities
- Anticoagulation therapy
- Cancer history including breast cancer.