NCT06204354

Brief Summary

Constructing a gynecological tumor samples library, which is open and can be accessed.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
2,500

participants targeted

Target at P75+ for all trials

Timeline
7mo left

Started Jan 2024

Typical duration for all trials

Status
not yet recruiting

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

Study Progress82%
Jan 2024Jan 2027

First Submitted

Initial submission to the registry

December 22, 2023

Completed
10 days until next milestone

Study Start

First participant enrolled

January 1, 2024

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 12, 2024

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2027

Last Updated

January 12, 2024

Status Verified

December 1, 2023

Enrollment Period

3 years

First QC Date

December 22, 2023

Last Update Submit

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

Age18 Years - 80 Years
Sexfemale
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

Retention: SAMPLES WITH DNA

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