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A Single-center, open controlled study for the need of systemic para-aortic and pelvic lymphadenectomy in elderly patients with advanced ovarian cancer reduction surgery

A Single-center, open controlled study for the need of systemic para-aortic and pelvic lymphadenectomy in elderly patients with advanced ovarian cancer reduction surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021880
Enrollment
Unknown
Registered
2019-03-14
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-03-18

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

Conditions

Ovarian Cancer

Interventions

test group:Selective cleanup of lymph nodes
control group:Systemic cleanup of lymph nodes

Sponsors

Shengjing Hospital affiliated to China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Subjects aged 60 to 75 years. 2. Initial surgical treatment (general staging or cytoreductive surgery) that has been histologically diagnosed and standardized. 3. Postoperative stage is II to IVA (segment according to 2014 FIGO staging standard). 4. Give the greatest degree of tumor cytoreductive surgery as far as possible to achieve R0 or R1. 5. The pathological type is epithelial ovarian cancer, fallopian tube cancer or peritoneal cancer. 6. For patients with stage III to IV who have large tumors and are unable to achieve satisfactory tumor reduction or have a high risk of surgery, neoadjuvant chemotherapy may be considered, followed by intermittent cytoreductive surgery. 6) At least 4-6 courses of platinum-based chemotherapy after surgery. 7) KPS physical status score = 60. 8) The estimated survival time is =12 weeks. 9) Complete objective imaging examinations such as abdominal CT/MR/PETCT before surgery. 10) Subjects have signed an informed consent form prior to conducting a specific study operation or evaluation and are willing to receive treatment and follow-up according to the protocol.

Exclusion criteria

Exclusion criteria: 1. Severe coagulation mechanism disorder, bleeding tendency. 2. The subject has any serious and/or pre-existing unstable disease (eg, uncontrolled infection, etc.), mental illness or safety of the subject, signing informed consent or compliance with the protocol. The situation of influence. 3. There are other contraindications for surgery and chemotherapy. 4. The investigator believes that it is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
3-year survival rate;5-year survival rate;

Countries

China

Contacts

Public ContactXiuqin Li

Department of Gynecology, Shengjing Hospital affiliated to China Medical University

2403621353@qq.com+86 18940251286

Outcome results

None listed

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