Intraperitoneal Chemotherapy in Recurrent Ovarian Cancer

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20+
SponsorFar Eastern Memorial Hospital

About this trial

This study aims to compare intravenous chemotherapy versus intraperitoneal chemotherapy in patients with recurrent ovarian cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

women who had recurrent ovarian cancer and was treated with either intravenous or intraperitoneal platinum based chemotherapy

Disqualifiers

women who did not complete the designated treatment course (exception to those who had to quit due to progressive disease or death of any cause)

Trial population

woman with recurrent ovarian cancer who was treated with chemotherapy (either intravenous or intraperitoneal)

Trial design

Design model

Case-control

Time perspective

Retrospective

Treatments tested in this trial

  • Chemotherapy

    Drug

    Intravenous chemotherapy versus intraperitoneal chemotherapy in recurrent ovarian cancer

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: intravenous chemotherapy1 intervention
Group B: intraperitoneal chemotherapy1 intervention

Trial outcomes

Primary outcomes

1

RFS

Recurrence free survival

Time frame
the time interval from the date of surgery or the start of chemotherapy to clinically defined recurrence, disease progression, death from any cause or last follow-up
2

OS

Overall Survival

Time frame
the time interval from the date of surgery or the start of chemotherapy to the date of death from any cause or last follow-up

Secondary outcomes

Other outcomes

Sponsors and contacts

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