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Spots Global Cancer Trial Database for MRI and PET Imaging in Predicting Treatment Response in Patients With Stage IB-IVA Cervical Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: MRI and PET Imaging in Predicting Treatment Response in Patients With Stage IB-IVA Cervical Cancer

Official Title: MRI- and PET-Predictive-Assay of Treatment Outcome in Cancer of the Cervix

Study ID: NCT01992861

Study Description

Brief Summary: This trial studies magnetic resonance imaging (MRI) and positron emission tomography (PET) imaging in predictive treatment response in patients with stage IB-IVA cervical cancer. MRI is a procedure in which radio waves and a powerful magnet linked to a computer are used to create detailed pictures of areas inside the body. PET is a procedure in which a small amount of radioactive glucose (sugar) is injected into a vein, and a scanner is used to make detailed, computerized pictures of areas inside the body where the glucose is taken up. Comparing results of diagnostic procedures, such as MRI and PET, done before, during and after radiation and chemotherapy may help doctors predict a patient's response to treatment and help plan the best treatment.

Detailed Description: OUTLINE: Patients undergo radiation therapy and receive chemotherapy per standard of care. Patients undergo dynamic contrast-enhanced (DCE) MRI, diffusion-weighted (DW) MRI, and magnetic resonance (MR) spectroscopy at baseline, 2-2.5 weeks, 4-5 weeks, and 1 month following radiation therapy completion, and fludeoxyglucose F 18 (FDG) PET/computed tomography (CT) at baseline, 2-2.5 weeks, and 4-5 weeks. After completion of study, patients are followed up at least every 3-6 months for 5 years.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

University of Miami Miller School of Medicine-Sylvester Cancer Center, Miami, Florida, United States

Loyola University Medical Center, Maywood, Illinois, United States

Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States

Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington, United States

University of Toronto, Toronto, Ontario, Canada

University of Hong Kong, Hong Kong, , Hong Kong

Contact Details

Name: Simon Lo

Affiliation: Fred Hutch/University of Washington Cancer Consortium

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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