Skip to content

Different low doses of mifepristone in the treatment of adenomyosis with dysmenorrhea: a non-randomized controlled study

Evaluation of Therapeutic Effect and Safety of RU-486 in the Treatment of Adenomyosis and Endometriosis

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015514
Enrollment
Unknown
Registered
2018-04-04
Start date
2015-12-01
Completion date
Unknown
Last updated
2020-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

endometriosis and adenomyosis

Interventions

1:2.5mg qd
2:5mg qd
3:25mg qw

Sponsors

Women's Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) female, aged >=18, menstruating,agree to the RU - 486 treatment and signed informed consent; (2) the preoperative vaginal ultrasound and/or nuclear magnetic resonance (MRI) confirmed as a diffuse wall after the front wall of the uterus, and/or glandular myopathy, cause myometrium diffuse thickening obviously; (3) severe dysmenorrhea or with menorrhagia; (4) placed separately LNG-IUS invalid or failure, including oral contraceptive drugs; (5) requires the uterus or fertility; (6) 3 months before drug treatment, did not accept other hormonal drug therapy for adenomyosis.

Exclusion criteria

Exclusion criteria: 1. participating in other clinical trials of patients; 2. the researchers think the other reasons are not suitable for clinical subjects, as follows: (1) the endometrium cervical breast malignant diseases; (2) with serious heart, liver, kidney function disorder and so on; (3) according to the researchers evaluation, the existing patients may as a result of the drug treatment and disease; (4) pregnancy or lactation in the three months before the start of treatment had childbirth, abortion or lactation); (5) going to pregnancy within the established treatment period or give birth,miscarriage, lactation 3 months before treatment; (6) body mass index (BMI) > 30 kg/m2; (7) allergic to study drug ingredients; (8) Combination using other drugs.

Design outcomes

Primary

MeasureTime frame
pain;menstrual amount;the volume of uterus;CA125;hemoglobin;endometrial thickness;

Countries

China

Contacts

Public ContactXinmei Zhang

Women's Hospital School Of Medicine Zhejiang University

zxm20130729@163.com+86 13957168298

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026