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Clinical screening and analysis of optimal placement of Mirena in patients with adenomyosis

Clinical screening and analysis of optimal placement of Mirena in patients with adenomyosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094164
Enrollment
Unknown
Registered
2024-12-17
Start date
2024-12-30
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

adenomyosis

Interventions

1 group:none
2 group:None

Sponsors

Hubei Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with adenomyopathy (disease) first diagnosed by US and/or MRI (diagnostic criteria: myometrial cyst, distorted and uneven myometrial echo structure, abnormal myometrial echo structure lesions with blurred boundaries, spherical and/or asymmetrical uterus); 2, >=18 years old, premenopausal or strongly want to preserve fertility; 3, unbearable dysmenorrhea or abnormal uterine bleeding, excessive menstruation. 4. There was no history of medium-dose hormone pills, GnRH agonists (GnRHa), testosterone derivatives, estrogen antagonists, aromatase inhibitors, DNG, or other progesterone or surgical treatment prior to inclusion. 5. No indications for surgery.

Exclusion criteria

Exclusion criteria: 1. Electronic medical record data is incomplete. 2. Lost follow-up after implantation. 3. Try to get pregnant after implantation. 4. There are indications for surgery. 5, uterine malformations, chronic pelvic inflammatory disease, ovarian tumors, other endocrine diseases, coagulation abnormalities or active thrombotic diseases, moderate to severe anemia, cardiovascular diseases, liver and kidney dysfunction and sexual function dependent malignancies. 6. Current pregnancy and lactation period. 7. Receive hormone therapy within 3 months before starting treatment. 8. Unexplained genital bleeding (vaginal or vulva). 9. Any contraindications to LNG-IUS placement, previous adenomyosis surgery, postmenopausal status, or patient refusal to participate.

Design outcomes

Primary

MeasureTime frame
dysmenorrhea;menstrual blood volume;focal size;

Countries

China

Contacts

Public ContactTongfu Feng

Hubei Maternal and Child Health Hospital, Huazhong University of Science and Technology

ftfsunny@163.com+86 189 8612 3645

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026