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Predicting Outcome in Cervix Carcinoma: a Prospective Study (POCER)

M

Maastricht Radiation Oncology

Status

Completed

Conditions

Cervical Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT01825005
12-4-008

Details and patient eligibility

About

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.

Enrollment

423 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

423 participants in 4 patient groups

group 1:surgery
Description:
treatment = surgery only
group 2: radiotherapy
Description:
treatment = radiotherapy only
group 3: RT and CT, and/or hyperthermia
Description:
treatment= radiotherapy combined with chemotherapy and/or hyperthermia
group 4: stage IVb , any treatment
Description:
cervical cancer stage IV b, treatment = any systemic or radiation therapy and supportive care

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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