Clinicopathologic and Ancillary Testing of Primary Clear Cell Carcinoma of the Cervix

Part of paid clinical trials in Houston, Texas.

Sponsor
M.D. Anderson Cancer Center
Study ID
NCT05046080
Status
Recruiting

Conditions

  • Human Papillomavirus-Independent Cervical Adenocarcinoma, Clear Cell-Type

Eligibility Criteria

Sex
FEMALE
Age
N/A - N/A
Healthy Volunteers
Not accepted

Interventions

  • Electronic Health Record Review — OTHER
    Medical records reviewed
  • Laboratory Biomarker Analysis — OTHER
    Correlative studies

Study Details

This study aims to provide a comprehensive report on clinicopathologic features, immunohistochemical/biomarker testing and molecular profile of cervical clear cell carcinoma. This study may help researchers learn more about the molecular profile of cervical clear cell carcinoma.

Key Dates

Start date
Aug 6, 2021
Status verified
Feb 2026
Primary completion
Sep 29, 2026
Completion
Sep 29, 2026

Study Design

Enrollment
70 participants (estimated)

Arms

  • Arm: Observational (medical record review)
    Patients' medical records are reviewed retrospectively, and archival tumor tissue analyzed by immunohistochemistry and next generation sequencing.

Primary Outcome Measure

Clinicopathologic study on patients diagnosed and treated for clear cell carcinoma of the cervix [ Time Frame: through study completion, an average of 1 year ]

Locations (1)

FacilityCityStateZIPSite coordinators
M D Anderson Cancer CenterHoustonTexas77030
Anasis Malpica
713-792-4655
Anasis Malpica (PRINCIPAL_INVESTIGATOR)

Find similar trials in Houston, TX