Clinical trial

Clinical Experience of Dienogest in Perimenopausal Females With Symptomatic Adenomyosis

Name
202207140RINB
Description
Between September 2018 and December 2021, women who did not want further childbearing and received dienogest treatment for dysmenorrhea and/or hypermenorrhea were included in a retrospective chart review. Dienogest 2mg was prescribed once per day orally after completing the above-mentioned exam. The patient would return to our clinic on the 1st, 3rd, and 6th then every 3 months for a prescription. The primary outcome was successfully long-term (more than a year) dienogest use for pain and/or bleeding control. The secondary outcomes were the reasons for discontinuing dienogest treatment and the predictor of successful long-term treatment.
Trial arms
Trial start
2018-09-01
Estimated PCD
2021-12-31
Trial end
2021-12-31
Status
Completed
Treatment
Dienogest
Dienogest 2mg was prescribed once per day orally
Arms:
Women with adenomyosis under dienogest
Other names:
Visanne, Bayer
Size
87
Primary endpoint
1 year dienogest use
September 2018 and December 2021
Eligibility criteria
Inclusion Criteria: * Women with adenomyosis who did not want further childbearing and received dienogest treatment for dysmenorrhea and/or hypermenorrhea Exclusion Criteria: * \< 40 y/o * Post-operative prevention of endometriosis recurrence * Medical conditions not suitable for dienogest treatment, such as known breast cancer, high thromboembolic effect, and smoking
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'RETROSPECTIVE'}, 'enrollmentInfo': {'count': 87, 'type': 'ACTUAL'}}
Updated at
2023-03-02

1 organization

1 product

2 indications

Product
Dienogest
Indication
Adenomyosis
Indication
Adherence