Radical Trachelectomy for Women With Early Stage Cervical Cancer

Status unconfirmed

Conditions studied: Cervical Cancer

In brief

The goal of this research study is to learn about quality of life, sexual functioning, and symptoms in women who have undergone abdominal radical trachelectomy for cervical cancer. This is an investigational study. Up to 100 patients will be enrolled in this study. All will be enrolled at MD Anderson.

Key facts

Study ID

NCT00813007

Run by

M.D. Anderson Cancer Center

People needed

50

Starts

2008-12-16

Expected to finish

2020-12-31

Last updated by the study team

2020-01-23

Who can join

Age: 18 and older, up to 40. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women with histologically confirmed, primary adenocarcinoma, squamous cell carcinoma or adenosquamous carcinoma of the uterine cervix
• Patients with FIGO stage IA1 (with lymph vascular space invasion), IA2, or IB1 disease
• Patients must be suitable candidates for surgery
• Patients who have signed an approved Informed Consent
• Patients with a prior malignancy allowed if > 3 years previous with no current evidence of disease
• Females older than 18 years who are undergoing radical trachelectomy
• Women must be able to read and write in either Spanish or English

You may not qualify if…

• Any histological type other than adenocarcinoma, squamous cell carcinoma or adenosquamous carcinoma of the uterine cervix
• Tumor size greater than 4 cm
• FIGO stage II-IV disease
• Patients with a history of pelvic or abdominal radiotherapy
• Patients who are pregnant
• Patients with contraindications to surgery
• Patients with evidence of metastatic disease by conventional imaging studies, enlarged pelvic or aortic lymph nodes > 2cm; or histologically positive lymph nodes

Where it is running

• University of Texas MD Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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