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A multicenter randomized controlled study about Levonorgestrel-releasing intrauterine device suture in the treatment of adenomyosis

A multicenter randomized controlled study about Levonorgestrel-releasing intrauterine device suture in the treatment of adenomyosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071520
Enrollment
Unknown
Registered
2023-05-17
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

adenomyosis

Interventions

LNG-IUS suture fixation:Hysteroscopic fixation of Manyule ring
simple placement of LNG-IUS:Simple Manyue Music Ring Placement

Sponsors

Hangzhou First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1:She had menorrhagia or dysmenorrhea and met the diagnosis of "adenomyosis"; 2:She had a strong desire to preserve the uterus; 3:She had no fertility requirements in the short term.

Exclusion criteria

Exclusion criteria: 1: She existed contraindications to use of the LNG-IUS; 2: She existed contraindications to hysteroscopic surgery; 3: She had other diseases of the reproductive tract (malignant tumors, deformities, or acute infections); 4: She had severe heart, lung, liver, and kidney insufficiency; 5: She had received gonadotropin-releasing hormone a (GnRG-a) treatment within the previous 6 months; 6: She refused to participate in this study.

Design outcomes

Primary

MeasureTime frame
LNG-IUS expulsion rate;—

Secondary

MeasureTime frame
algomenorrhea;Menstrual volume;side effects;CA125;—

Countries

China

Contacts

Public ContactJinyi Tong

Hangzhou First People's Hospital

tongjinyi252@zju.edu.cn+86 135 8881 8180

Outcome results

None listed

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