Construction of Gynecological Tumor Sample Library
1 other identifier
observational
2,500
0 countries
N/A
Brief Summary
Constructing a gynecological tumor samples library, which is open and can be accessed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2024
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 22, 2023
CompletedStudy Start
First participant enrolled
January 1, 2024
CompletedFirst Posted
Study publicly available on registry
January 12, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2027
January 12, 2024
December 1, 2023
3 years
December 22, 2023
January 10, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
construction of Biobank
Biobank including gynecolgic cancer samples, including cervical cancer, endometrial cancer, ovarian cancer, vulva cancer, vaginal cancer, and others types
3 years
Secondary Outcomes (2)
Exploring the molecular mechanism based on biobank
3 year
Drug sensitivity detection based on biobank
3 year
Study Arms (6)
samples of cervical cancer
fresh samples collected from patients diagnosed with cervical cancer
samples of endometrial cancer
fresh samples collected from patients diagnosed with endometrial cancer
samples of ovarian cancer
fresh samples collected from patients diagnosed with ovarian cancer
samples of vulva cancer
fresh samples collected from patients diagnosed with vulva cancer
samples of vaginal cancer
fresh samples collected from patients diagnosed with vaginal cancer
samples of rare gynecological cancer
fresh samples collected from patients diagnosed with rare gynecological cancer
Eligibility Criteria
Patients diagnosed with gynecologic cancer, including cervical cancer, endometrial cancer, ovarian cancer, vulva cancer, vaginal cancer, and other rare type gynecologic cancer.
You may qualify if:
- An informed consent form was obtained. If the age is less than 18 years old, the consent form should be signed by the guardian.
- Preoperative tumor burden assessment and intraoperative evaluation by the supervising physician (professor) suggest sampling is acceptable.
- The research team believes that sampling is possible.
- Having the relevant requirements for sample library storage.
- Surgical treatment is performed at Peking Union Medical College Hospital.
You may not qualify if:
- The research team considers any circumstances or considerations that may hinder normal pathological evaluation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Biospecimen
Fresh samples from gynecological cancer, including cervical cancer, ovarian cancer, endometrial cancer, vulva cancer, vaginal cancer, and some other rare type of cancer.
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 22, 2023
First Posted
January 12, 2024
Study Start
January 1, 2024
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
January 1, 2027
Last Updated
January 12, 2024
Record last verified: 2023-12