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Exploration of a new treatment model for newly diagnosed advanced epithelial ovarian cancer - A phase II Trial

Exploration of a new treatment model for newly diagnosed advanced epithelial ovarian cancer - A phase II Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048625
Enrollment
Unknown
Registered
2021-07-11
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

Advanced epithelial ovarian cancer

Interventions

Surgery Group:A certain degree of cytoreductive surgery with adjuvant chemotherapy
Ccontrol Group:Neoadjuvant chemotherapy with interval debulking surgery

Sponsors

Obstetrics and Gynecology Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years; 2. Histopathologically diagnosed as advanced epithelial ovarian cancer; 3. After clinical evaluation, the initial operation cannot reach R0 or R1; 4. Unbearable systemic symptoms such as extreme fatigue, unexplained pain, dyspnea, repeated bleeding, or local symptoms such as obstruction, rupture, and obvious compression due to large tumor burden; laboratory tests show coagulation dysfunction, systemic inflammatory response or cardiac , liver, brain, lung, kidney and other important organ dysfunction; imaging examination showed extensive tumor metastasis; 5. Have not received any surgical treatment related to the disease before this study; 6. Those who have no contraindications to intravenous chemotherapy; 7. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with recurrent ovarian cancer; 2. Have received surgical treatment related to the disease; 3. Combined with other malignant diseases; 4. Mental illness or mental illness, unable to cooperate with the experiment; 5. Patients whose family members request to conceal their illness; 6. Participate in other clinical trials at the same time.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Mortality at 30 days after surgery;the incidence of perioperative complications;Progression Free Surviva;

Countries

China

Contacts

Public ContactYao Liangqing

Obstetrics and Gynecology Hospital Affiliated to Fudan University

yaoliangqing@163.com+86 13916644444

Outcome results

None listed

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