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 — OTHERMedical records reviewed
- Laboratory Biomarker Analysis — OTHERCorrelative 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)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| M D Anderson Cancer Center | Houston | Texas | 77030 | Anasis Malpica (PRINCIPAL_INVESTIGATOR) |
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