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Clinical Trials/NCT05813509
NCT05813509
Recruiting
Not Applicable

Chief Physician of Obstetrics and Gynecology Department of the First Affiliated Hospital of Xiamen University

The First Affiliated Hospital of Xiamen University1 site in 1 country30 target enrollmentDecember 1, 2022
ConditionsOvarian Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ovarian Cancer
Sponsor
The First Affiliated Hospital of Xiamen University
Enrollment
30
Locations
1
Primary Endpoint
Objective remission rate
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The research purpose of this study is to use organoid cultured from patients' own ovarian cancer tissues as models, screen potential clinical therapeutic drugs (such as paclitaxel, gemcitabine, etc.) in vitro, formulate individualized drug treatment plans for individual patient, and evaluate the clinical application value of organ like drug sensitivity technology.

Detailed Description

Under the guidance of ultrasound, the lesions were punctured to obtain tumor cells; The cells were amplified and cultured by organ like culture method to establish ovarian cancer like organoid. The drug sensitivity tests of different drugs were carried out on similar organs. Number of drugs tested: 10 (paclitaxel, carboplatin, lobaplatin, doxorubicin, etc.); After the test is completed, sufficient chemotherapy for full course of treatment shall be carried out according to the drug sensitivity results; After chemotherapy, blood and imaging evaluation were performed; Collect the information of patients from initial treatment to the end of chemotherapy; Matching the corresponding number of patients with platinum resistant relapse who did not undergo organ like culture; At each end point, the evaluation and comparison were carried out and the research conclusions were drawn.

Registry
clinicaltrials.gov
Start Date
December 1, 2022
End Date
February 1, 2025
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Objective remission rate

Time Frame: 6 months

partial or complete remission ratio according to RECIST criteria

Secondary Outcomes

  • Progression free survival(3 years)

Study Sites (1)

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