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Early patients with endometrial cancer and endometrial atypical hyperplasia of reproductive function related research

Early patients with endometrial cancer and endometrial atypical hyperplasia of reproductive function related research

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OON-16008470
Enrollment
Unknown
Registered
2016-05-13
Start date
2016-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Early endometrial cancer and endometrial atypical hyperplasia

Interventions

Study of A1 group:Oral high progesterone
Study of A2 group:Intrauterine placed LNG-IUS
Study of B1 group:Segmental tylectomy under hysteroscope + consolidation therapy of highly active progesterone
Study of B2 group:Segmental tylectomy under hysteroscope + consolidation therapy of LNG-IUS
control group:Hysterosalpingo-oophorectomy

Sponsors

Women and Children Hospital of Northwest
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Aged 40 years old or less, not producing or strong desire for fertility; 2. histologically confirmed is the IA stage (FIGO), high differentiation of endometrial adenocarcinoma; 3. the immunohistochemical female progesterone receptor positive; 4. except the ultrasound and MRI myometrium invasion or evidence of cervical involvement, no outside uterine lesions lymph nodes and distant metastasis; 5. Serum CA125 is normal and <35KU/L; 6. excluding cardiopulmonary dysfunction, acute injury of liver and kidney function, blood coagulation dysfunction, such as system disease, no taboo drug treatment; 7. merged to exclude hereditary colorectal polyps sex (ereditary non - polyposis colorectal cancer, HNPCC) family history, history of other tumors or combined with other parts of the tumor; 8. conditional close follow-up, good adherence, subjects were informed consent and voluntary access to the clinical trials.

Exclusion criteria

Exclusion criteria: 1. Complicated with cardiovascular, hepartic, renal and hematopoietic disease or other malignant tumor; 2. With poor compliance and difficult to follow-up; 3. Participating in other trials at the same time; 4. Other conditions improper for the trial.

Design outcomes

Primary

MeasureTime frame
Treatment of working time;Complete response time;time to recurrence;remission rate;recurrence rate;Disease-free survival;The pregnancy rate after treatment to ease;expression quantity of PR-A;expression quantity of PR-B;expression quantity of PR-M;expression quantity of TRL4;

Secondary

MeasureTime frame
parturition rate;

Countries

China

Contacts

Public ContactYanni Tian

The Northwest Women and Children Hospital

cwatyn2008@163.com+86 15389440581

Outcome results

None listed

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