NCT06317610

Brief Summary

The present study aims to collect early bright field image of patient-derived organoids with ovarian cancer. By leveraging artificial intelligence, this study will seek to construct and refine algorithms that able to predict growth of ovarian cancer organoids.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2022

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

March 12, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 19, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 30, 2024

Completed
Last Updated

March 19, 2024

Status Verified

March 1, 2024

Enrollment Period

2.3 years

First QC Date

March 12, 2024

Last Update Submit

March 12, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • AUC of growth prediction performance using deep learning model

    AUC =Area under receiver operating characteristic curve

    up to 3 years

  • Accuracy of growth prediction using deep learning model

    Accuracy=( the number of correctly classified samples)/( the number of total samples)

    up to 3 years

Interventions

biopsy or puncture: Patients received biopsy or puncture to obtain tumor tissues or Malignant effusion for organoids establishment

Eligibility Criteria

Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsOnly women get ovarian cancer
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with epithelial ovarian cancer received biopsy or puncture to obtain tumor tissues or malignant effusion

You may qualify if:

  • Patients must have histologically confirmed diagnosis of epithelial ovarian cancer
  • Patients received biopsy or puncture to obtain tumor tissues or malignant effusion
  • Patients voluntarily participated in the study and signed informed consent.

You may not qualify if:

  • Non-epithelial ovarian cancer
  • No sufficient amount of tumor tissues or malignant effusion for organoids establishment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chongqing Cancer Hospital

Chongqing, Chongqing Municipality, 400030, China

RECRUITING

MeSH Terms

Conditions

Ovarian Neoplasms

Condition Hierarchy (Ancestors)

Endocrine Gland NeoplasmsNeoplasms by SiteNeoplasmsOvarian DiseasesAdnexal DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Neoplasms, FemaleUrogenital NeoplasmsGenital DiseasesEndocrine System DiseasesGonadal Disorders

Study Officials

  • Dongling Zou, M.D.

    Chongqing University Cancer Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Dongling Zou, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 12, 2024

First Posted

March 19, 2024

Study Start

January 1, 2022

Primary Completion

April 30, 2024

Study Completion

May 30, 2024

Last Updated

March 19, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

Locations