Zhongshan Hospital, Fudan University
Shanghai, China
Location status: Recruiting
NCT Number: NCT05236686
The purpose of this study is to evaluate the safety and the effectiveness of hepato-celiac lymphadenectomy in the treatment of primarily diagnosed advanced epithelial ovarian cancer and platinum-sensitive recurrent ovarian cancer.
Interested in participating?
Request Info18 year–75 year
Female
Interventional
Not applicable
Shanghai, China
Location status: Recruiting
This single-arm, multi-center, phase II trial is to evaluate the safety and effectiveness of hepato-celiac lymphadenectomy in the treatment of ovarian cancer with hepato-celiac lymph nodes metastases, in the circumstance of primarily diagnosed advanced epithelial ovarian cancer (primary debulking surgery or interval debulking surgery) and of platinum-sensitive recurrent ovarian cancer (no more than 4 lines of therapy).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Hepato-celiac lymphadenectomy in the treatment of epithelial ovarian cancer, with a maximum cytoreduction, in the circumstance of primarily diagnosed advanced epithelial ovarian cancer (primary debulking surgery or interval debulking surgery) and of platinum-sensitive recurrent ovarian cancer (no more than 4 lines of therapy).
Time frame: Participants will be followed up to 2 years after randomization
The proportion of patients without disease progression or death at 2 years after entry into the study.
Time frame: Participants will be followed up to 24 months after randomization
The time from entry into the study to the diagnosis of the first progression or recurrence or death, whichever occurs first
Time frame: Participants will be followed up to 60 months after randomization
The time from date of randomization until the date of death from any cause or last follow-up
Time frame: Participants will be followed up to 24 months after randomization
The proportion of patients who achieved complete response (CR) or partial response (PR)
Time frame: Participants will be followed up to 24 months after randomization
The proportion of patients who achieved complete response (CR) or partial response (PR) or stable disease (SD)
Time frame: Participants will be followed up to 90 days after randomization
Postoperative 30-day, 60-day and 90-day complications
Time frame: Baseline; 6 months, 12 months and 24 months after randomization
Assessment of potential impact of first line treatment on functionality and well-being in patients by the EORTC core quality of life questionnaire (QLQ-C30, version 3.0).
Time frame: Baseline; 6 months, 12 months and 24 months after randomization
Assessment of potential impact of first line treatment on functionality and well-being in patients by functional assessment of cancer therapy-ovary (FACT-O, version 4).
Time frame: Participants will be followed up to 24 months after randomization
The number and sites of subsequent recurrence, including pelvic, abdominal, retroperitoneal lymph nodes, hepato-celiac lymph nodes and distant metastases and ascites, etc.
Contact information is provided by the study sponsor or research team.
Shanghai Gynecologic Oncology Group
Other Gov
A Prospective, Multi-center, Single-Arm Phase II Clinical Study to Evaluate Safety and Effectiveness of Hepato-celiac Lymphadenectomy in the Treatment of Advanced and Recurrent Ovarian Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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