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The application of internal iliac artery infusion chemotherapy in patients with advanced ovarian cancer

The application of internal iliac artery infusion chemotherapy in patients with advanced ovarian cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONN-17014070
Enrollment
Unknown
Registered
2017-12-21
Start date
2018-01-01
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

Ovarian Cancer

Interventions

Control Group:(Paclitaxel + cisplatin) intravenous chemotherapy
Group 1:(Paclitaxel + cisplatin) intravenous chemotherapy plus arterial infusion of cisplatin (the second, fourth and sixth cycle)

Sponsors

The Obstetrics & Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) 100 cases of advanced ovarian cancer (stage III - IV) treated by tumor reduction surgery and confirmed by pathology; 2) before the study, we did not receive any treatment related to this disease, including surgery, hormone therapy (cyclical treatment, etc.), chemotherapy, radiotherapy and other antitumor drugs. There was no contraindication between intravenous chemotherapy and interventional chemotherapy; 3) the signing of the informed consent; 4) any one in conformity with the following exclusion criteria is not included.

Exclusion criteria

Exclusion criteria: 1) patients with advanced ovarian cancer are in a life - threatening emergency; 2) the combination of other malignant diseases; 3) younger than 18 years) or elderly (over 70 years) or for other reasons can't sign the informed consent, and no other guardian agent; 4) mental illness or psychological illness, unable to cooperate with the experimenter; 5) need to hide the disease for the patient; 6) take part in other clinical trials at the same time.

Design outcomes

Primary

MeasureTime frame
CA125;immunohistochemistry;HE4;ultrasonography;time to live;Liver and kidney function;

Countries

China

Contacts

Public ContactLiangqing Yao

The Obstetrics & Gynecology Hospital of Fudan University

yaoliangqing@163.com+86 13916644444

Outcome results

None listed

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