Clinical Database and Biobank of Patients With Gynecologic Neoplasms

Sponsor
Huazhong University of Science and Technology (Other)
Overall Status
Unknown status
CT.gov ID
NCT01267851
Collaborator
Zhejiang University (Other), Hunan Province Tumor Hospital (Other), Guangxi Medical University (Other), First Affiliated Hospital Xi'an Jiaotong University (Other), West China Second University Hospital (Other), Obstetrics & Gynecology Hospital of Fudan University (Other), Shanghai First Maternity and Infant Hospital (Other), Peking University People's Hospital (Other), Wuhan Central Hospital (Other)
1,600,000
1
131.9
12126.5

Study Details

Study Description

Brief Summary

The database and biobank establishment started in 1997 in our institute. However, the sample size was too small with respect to our clinical and fundamental scientific research's requirement. Thus the Chinese gynecological oncology study (GOS) group was established to create a large multicentre database and biobank of patients with gynecologic diseases.

Detailed Description

The database contains clinical and epidemiologic information about patients with gynecologic neoplasms, such as cervical carcinoma, ovarian carcinoma, etc. With the data gathered from this database, the investigators could further demonstrate the etiology, risk factor, clinical treatment, and other aspects of the complicated gynecologic diseases. The cervical cancer database v1.10 including more than 10,000 cases and more than 200 variables has been established.

The biobank collects blood, fluids, tissue samples, and related clinical data from consenting patients with gynecologic neoplasms, such as cervical cancer, ovarian cancer, endometrial cancer, choriocarcinoma, uterine myoma, endometriosis. Besides, blood samples of population-based healthy people with informed consent are also collected.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1600000 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
A Large Multicentre Clinical Database and Biobank of Patients With Gynecologic Neoplasms
Actual Study Start Date :
Jan 1, 2010
Anticipated Primary Completion Date :
Dec 30, 2019
Anticipated Study Completion Date :
Dec 30, 2020

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • patients with informed consent;

    • patients with gynecologic diseases;

    • patients with intact clinical and pathological information

    Exclusion Criteria:
    • not included in the inclusion criteria

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Tongji Hospital of HUST Wuhan Hubei China

    Sponsors and Collaborators

    • Huazhong University of Science and Technology
    • Zhejiang University
    • Hunan Province Tumor Hospital
    • Guangxi Medical University
    • First Affiliated Hospital Xi'an Jiaotong University
    • West China Second University Hospital
    • Obstetrics & Gynecology Hospital of Fudan University
    • Shanghai First Maternity and Infant Hospital
    • Peking University People's Hospital
    • Wuhan Central Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ding Ma, Director of the department of Obstetrics and Gynecology, Tongji Hospital, Huazhong University of Science and Technology
    ClinicalTrials.gov Identifier:
    NCT01267851
    Other Study ID Numbers:
    • GM2010-06-02
    First Posted:
    Dec 29, 2010
    Last Update Posted:
    Jul 19, 2019
    Last Verified:
    Jul 1, 2019
    Keywords provided by Ding Ma, Director of the department of Obstetrics and Gynecology, Tongji Hospital, Huazhong University of Science and Technology
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 19, 2019