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Clinical Database and Biobank of Patients With Gynecologic Neoplasms

A Large Multicentre Clinical Database and Biobank of Patients With Gynecologic Neoplasms

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01267851
Enrollment
1600000
Registered
2010-12-29
Start date
2010-01-01
Completion date
2020-12-30
Last updated
2019-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Cancer, Choriocarcinoma, Endometrial Cancer, Endometriosis, Ovarian Cancer, Uterine Myoma

Keywords

gynecologic disease

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.

Interventions

None listed

Sponsors

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

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
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

Countries

China

Contacts

Primary ContactMa Ding, M.D.
dma@tjh.tjmu.edu.cn86-27-8362681

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026