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NCT Number: NCT05251883

A Study to Analyze Data on Metastatic Ovarian Cancer Using Multi-omics

As one of the most common malignant tumors in women, the incidence of ovarian cancer is expected to increase year by year. Due to its lack of typical symptoms and effective screening methods, and the characteristics of implantation and distant metastasis, more than 70% of ovarian cancers were in the metastatic stage at the time of diagnosis. In this study, the investigators will collect large samples of tissue from patients with ovarian cancer, conduct multi-omics studies, and mapped the characteristic maps of the genome and transcriptome of patients with metastatic ovarian cancer, and explore the molecular mechanisms that can be used as new targets for the treatment of ovarian cancer. Besides, the investigators will design and establish a database of metastatic ovarian cancer, integrate multiple omics, imaging, pathology, and clinical information to study their potential relevance, and analyze the relationship between various omics, imaging, pathology, and prognosis, establish ovaries Cancer prediction model.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

The Sun Yat-Sen Memorial Hospital of Sun Yat-Sen Universit

Guangzhou, Guangdong, China

Location status: Recruiting

Location contact

Huaiwu Lu, associate professor

CONTACT

[email protected]

+8618688395806

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • female, ≥18 years old;
  • diagnosed as ovarian cancer by imaging and pathology;
  • did not receive any anti-tumor drug treatment before surgery in the gynecology clinical department of the Sun Yat Sen Memorial Hospital of Sun Yat-Sen University;
  • received ovarian cancer surgery and Follow-up treatment;
  • Patients voluntarily participate in the research of this subject, have good compliance, and can complete the enrollment by the requirements of the trial;
  • Sign informed consent and agree to the collection and use of their data.

Exclusion criteria

  • Patients who have received other anti-tumor treatments or received tumor surgery before enrollment;
  • Patients with malignant tumors in other parts;
  • Patients with uncontrollable neurological, psychiatric, or mental disorders;
  • Poor compliance and inability to Cooperate and describe treatment responders.

Treatment and study plan

Primary outcomes

  1. Progression-Free-Survival

    Time frame: The sample will be tested immediately after they are taken from patients and the statistical analysis will be taken through study completion, an average of 3 year

Study contacts

Contact information is provided by the study sponsor or research team.

Huaiwu Lu, Study Director

CONTACT

[email protected]

+86 18688395806

Sponsors and collaborators

Lead sponsor

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Other

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2026
First posted
Feb 23, 2022
Registry last updated
May 19, 2023

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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