Skip to content

Comparison of clinical efficacy and incidence of uterine bleeding with different doses of GnRH-a in the treatment of adenomyosis in different periods of the menstrual cycle

Comparison of clinical efficacy and incidence of uterine bleeding with different doses of GnRH-a in the treatment of adenomyosis in different periods of the menstrual cycle

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059548
Enrollment
Unknown
Registered
2022-05-04
Start date
2021-07-01
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Adenomyosis

Interventions

Group 1:A 10.8 mg goserelin acetate sustained-release implant is subcutaneously injected every 12 weeks, and a total of 1-2 injections are given according to the patients condition
Group 2:A 3.6 mg goserelin acetate sustained-release implant is subcutaneously injected every 4 weeks, and a total of 3-6 injections are given according to the patients condition

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with adenomyosis based on clinical assessment, ultrasound or magnetic resonance imaging (MRI); 2. Women aged 18-49 years; 3. With symptoms of dysmenorrhea and/or menorrhagia ; 4. With good compliance during treatment and can cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating patients; 2. Patients treated with GnRH-a within 3 months; 3. Patients who have received adenomyosis related surgical treatment or interventional treatment; 4. Patients with intrauterine Levonorgestrel intrauterine Sustained-release system (LNG-IUD); 5. Refuse to use GnRH-a; 6. Patients with probable or confirmed uterine malignancy; 7. Patients with GnRH-a contraindication.

Design outcomes

Primary

MeasureTime frame
Blood routine;Carbohydrate antigen-125;Uterine volume;Days and volume of uterine bleeding with different degrees;NRS (Numerical rating scale) pain score;Uterine bleeding rate per cycle after treatment;

Secondary

MeasureTime frame
Drug-related side effects;

Countries

China

Contacts

Public ContactWang Guoyun
wangguoy@sdu.edu.cn+86 18560081729

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026