Actively Recruiting
Establishing a Tumor Registry for Patients With Neuroendocrine Carcinoma of the Cervix
Led by M.D. Anderson Cancer Center · Updated on 2026-03-05
750
Participants Needed
1
Research Sites
1598 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study collects information and data on patients with neuroendocrine cervical cancer. Information from this study may be used to better understand the correlation between clinical data, such as patient characteristics, treatment, and disease outcomes, and overall patient outcomes.
CONDITIONS
Official Title
Establishing a Tumor Registry for Patients With Neuroendocrine Carcinoma of the Cervix
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with a personal history of cervical cancer with any neuroendocrine component, including small cell, large cell, or undifferentiated high-grade neuroendocrine carcinoma
- Patients at any stage of treatment, surveillance, or recurrence when joining the study
- Patients with all stages of cervical cancer
- Patients who do not speak English if accompanied by an institutional interpreter
- Patients treated at any facility, including M. D. Anderson Cancer Center
- Patients of any country and ethnic background
- Patients requesting to participate regardless of how they learned about the study
- Next of kin or legal representatives of deceased patients with neuroendocrine carcinoma of the cervix if they read and speak English
You will not qualify if you...
- Patients with other histologic subtypes of neuroendocrine carcinoma of the cervix, including typical and atypical carcinoid tumors
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
M D Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
L
Larissa A. Meyer, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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