Idiopathic Menorrhagia Clinical Trial
Official title:
MiCo - Mirena or Conventional Medical Treatment for Menorrhagia (MA0901)
The aim of this prospective, non-interventional post-marketing surveillance study is to obtain data on safety and efficacy of Mirena in treatment of heavy menstrual bleeding (Menorrhagia) under daily-life treatment conditions.For each patient, an initial visit and one to three follow-up visits after about 3, 6 and 12 months will be documented by the treating physician on the case report form. Observations include the patient's demographic parameters (date of birth, height, weight, race and smoking habits), previous contraceptives and menorrhagia treatment, gynaecological history, baseline menstruation, result of insertion, concomitant medications and diseases as well as menorrhagia symptoms. Overall treatment success will be evaluated at the end of treatment including number of weeks until improvement and reduction of menstrual bleeding with respect to duration and severity, and patient's satisfaction.
| Status | Completed |
| Enrollment | 1211 |
| Est. completion date | June 2011 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 18 Years to 45 Years |
| Eligibility |
Inclusion Criteria: - Women between the ages of 18-45 (inclusive) not intending to become pregnant during the next year - Women complaining of heavy menstrual bleeding over several consecutive cycles - Women without structural or histological abnormality of the uterus, or with fibroids less than 3 cm in diameter which are causing no distortion of the uterine cavity (eligible for pharmaceutical treatment according to the NICE guideline 2007) - Informed consent (where required by laws or regulations) Exclusion Criteria: - The contraindications and warnings of the respective Summary of Product Characteristics (Mirena®, combined oral contraceptives, oral/injectable progestogens, non-steroidal anti-inflammatory drug, or anti-fibrinolytic agent) must be followed. - Women taking hormone replacement therapy - Women with symptoms such as intermenstrual or post-coital bleeding, unless an endometrial biopsy has been performed and pathology excluded - Women with fibroids that are palpable abdominally or who have intra-cavity fibroids and/or whose uterine length as measured at ultrasound or hysteroscopy is greater than 12 cm (NICE guideline 2007) - Women on anticoagulative therapy or other treatment (including e.g. Copper IUD use) known to cause menorrhagia |
Observational Model: Case Control, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Bayer |
Albania, Bosnia and Herzegovina, Colombia, Croatia, Czech Republic, Jordan, Lebanon, Macedonia, The Former Yugoslav Republic of, Moldova, Republic of, Romania, South Africa, Syrian Arab Republic, Ukraine, Venezuela,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Cumulative continuation rate at 12 months stratified by history of previous treatment(s) for menorrhagia | 12 months | No | |
| Secondary | Bleeding pattern | 12 months | No | |
| Secondary | Patient satisfaction at end of documentation | 12 months | No | |
| Secondary | Impact of the therapy in terms of patient-reported health outcomes assessed using a validated questionnaire (Shaw RW et. al., British Journal of Obstetrics and Gynaecology, Vol 105(11), 1998.) | 12 months | No | |
| Secondary | Safety profile (adverse events) | 12 months | Yes |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT00868153 -
Mirena in Idiopathic Menorrhagia
|
N/A |