About this trial
A cohort establishment study of total management of ovarian cancer (including fallopian tube cancer and primary peritoneal cancer).
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients diagnosed with ovarian cancer (including fallopian tube cancer, primary peritoneal cancer) and intended to be treated in our hospital;
Can cooperate with later follow-up.
Disqualifiers
Patients with other malignant tumors or previous history of other malignant tumors;
Have cognitive impairment.
Trial population
Patients diagnosed with ovarian cancer (including fallopian tube cancer, primary peritoneal cancer) and intended to be treated in our hospital
Trial design
Cohort
Prospective
Treatments tested in this trial
No intervention
Other interventionNo intervention
Treatment groups
Trial outcomes
Primary outcomes
Progress Freesurvival (PFS)
The time from the start of treatment until the patient progresses further or dies.
Overall Survival (OS)
Measure the time from the start of treatment to the time of death.
Secondary outcomes
Occurrence of adverse reactions
All adverse events were recorded.
Sponsors and contacts
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