Predicting Outcome in Cervix Carcinoma: a Prospective Study
Conditions
Cervical Cancer
Conditions: official terms
Uterine Cervical Neoplasms
Conditions: Keywords
cervical cancer
Study Type
Observational [Patient Registry]
Study Phase
N/A
Study Design
Observational Model: Cohort, Time Perspective: Prospective
Overall Status
Recruiting
Summary
The main aim is to validate and improve the predictive model for survival and toxicity in patients with cervical cancer through multicentric prospective data collection. The data contain information on patient, tumor and treatment characteristics. For this study, additional health related QOL scores will be assessed using the EORTC Quality of Life Questionair-CX24 and C30. The long term aim, beyond this specific study, is to build a Decision Support System based on the predictive model validated in this study.
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: N/A
Minimum Age: 18 Years
Gender: Female
Criteria: Inclusion Criteria:

- histological or cytological proven cervical cancer

- informed consent according to national rules

Exclusion Criteria:

- no histological or cytological proven cervical cancer

- no informed consent according to national rules
Locations
Maastricht University Hospital
Maastricht, Netherlands
Status: Recruiting
Contact: L Lutgens, MD, PhD - +31 88 44 55 666 - ludy.lutgens@maastro.nl
Bloemfontein medicross
Bloemfontein, Free State, South Africa
Status: Recruiting
Start Date
February 2013
Completion Date
February 2018
Sponsors
Maastricht Radiation Oncology
Source
Maastricht Radiation Oncology
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page