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Survey on Patient Satisfaction Rate for Mirena Use in Heavy Menstrual Bleeding

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Bayer

Status

Completed

Conditions

Menorrhagia

Treatments

Drug: Levonorgestrel (Mirena, BAY86-5028)

Study type

Observational

Funder types

Industry

Identifiers

NCT00874653
14175
MA0711IT (Other Identifier)

Details and patient eligibility

About

The purposes of this study are:

  • To evaluate patient satisfaction for efficacy and tolerability of heavy menstrual bleeding treatment by Mirena.
  • To collect italian data for Mirena in clinical routine.

Enrollment

78 patients

Sex

Female

Ages

30 to 49 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women diagnosed with Idiopathic Menorrhagia and Mirena inserted for a period no longer than three months according to the assessment of the investigator and according to the international and national guidelines. These women should also accept to be on contraception during the time period that they have Mirena in situ
  • Body Mass Index = 18-30

Exclusion criteria

  • One or more of the following disorders: 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

Trial design

78 participants in 1 patient group

Group 1
Treatment:
Drug: Levonorgestrel (Mirena, BAY86-5028)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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