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CIN clinical trials

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NCT ID: NCT00339989 Completed - Cervical Cancer Clinical Trials

Cervical Cancer Early Endpoints and Determinants

Start date: September 12, 2003
Phase:
Study type: Observational

This study, conducted by the National Cancer Institute and the University of Oklahoma, will look for changes in cervix cells and other samples that may be signs of cervical disease. Human papilloma virus, or HPV, is a common infection of the genitalia in women that usually goes away by itself. If HPV infection does not go away, it might turn into cancer of the cervix, although this is rare. This study will examine why many HPV infections go away and why a few persist and lead to cervical cancer. Women 18 years of age and older who are referred for colposcopy (examination of the vagina and cervix using an instrument with a magnifying lens) at the University of Oklahoma following Pap smear diagnosis may be eligible for this study. Women will be in one of the following diagnostic categories: - Cancer: Stage 1-2 only. - Precancer: Cervical intraepithelial neoplasia (CIN3). - HPV-infected: Positive for any of the 13 known cancer-causing HPV types, but not diagnosed with cancer or CIN3. - Normal: Negative for cancer-causing HPV and normal tissue laboratory results. Participants will undergo the following procedures: - Questionnaire: Covers demographic information (such as age, race, ethnicity, marital status, etc.), pregnancy history, menstrual and sexual history, contraceptive history, hormone medication history, medical history, smoking history, physical development, family history, and health care access. - Blood test: 2 tablespoons of blood drawn. - Colposcopy. - Procedure to collect a sample of cervical cells and fluids for HPV testing and research.

NCT ID: NCT00289029 Completed - CIN Clinical Trials

A Study of Two Iodinated Contrast Agents in Renally Impaired Patients Undergoing Cardiac Angiography

Start date: July 2005
Phase: Phase 4
Study type: Interventional

The main purpose of this study is to compare the incidence of contrast induced nephrotoxicity following the administration of Isovue or Visipaque in patients with moderate to severe renal insufficiency undergoing cardiac angiography. Serum creatinine will be measured before and up to 48-72 hours after the administration of the contrast agent to evaluate renal function.