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Spots Global Cancer Trial Database for Prediction of Clinical Response and Outcome in Uterine Cervix Cancer

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Trial Identification

Brief Title: Prediction of Clinical Response and Outcome in Uterine Cervix Cancer

Official Title: Predicting Clinical Response and Outcome After Definitive Irradiation With MRI-Guided Adaptive Brachytherapy in Uterine Cervix Cancer

Study ID: NCT01764217

Conditions

Cervix Cancer

Interventions

Study Description

Brief Summary: Observational study based on the routine clinical treatment and diagnostic course, to correlate imaging features with outcome objectives. Outcome will evaluated as clinical response to the standard treatment and as recurrence and survival in the follow up. The study hypothesis is that data extracted form FDG-PETCT used in the routine clinical practice can predict outcomes following standard treatment.

Detailed Description: This study will prospectively collect patients undergoing to the standard diagnostic and treatment protocol in Maastro Clinic. Any difference in the normal procedure will be adopted. The aim is to extrapolate form the PET images some features of the metabolic tumor activity to associate with different outcomes and tumor behaviours.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Philippe Lambin, Maastricht, Limburg, Netherlands

Contact Details

Name: philippe Lambin

Affiliation: Maastro Clinic, The Netherlands

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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