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Predicting Outcome in Cervix Carcinoma: a Prospective Study


N/A
18 Years
N/A
Open (Enrolling)
Female
Cervical Cancer

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Trial Information

Predicting Outcome in Cervix Carcinoma: a Prospective Study


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

Type of Study:

Observational [Patient Registry]

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

five-year overall survival rate

Outcome Description:

assessment of the overall survival 5 years after treatment

Outcome Time Frame:

5 years after treatment

Safety Issue:

No

Principal Investigator

P Lambin, Prof

Investigator Role:

Principal Investigator

Investigator Affiliation:

Maas tricht University hospital, dep of radiotherapy (Maastro clinic)

Authority:

Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)

Study ID:

12-4-008

NCT ID:

NCT01825005

Start Date:

February 2013

Completion Date:

February 2018

Related Keywords:

  • Cervical Cancer
  • cervical cancer
  • Carcinoma
  • Uterine Cervical Neoplasms

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