Recruiting NCT02733289
Standard Follow-up Program Cervix Cancer (SFP CERVIX)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Cervical Cancer Radiation Complications. Basic parameters: No limits · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Netherlands
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
Standard evaluation and follow-up data regarding complications of curative radiation treatment for cervical cancer.
Primary outcome measures
- Complications [Time frame: Five years]
Eligibility criteria
Inclusion criteria
- Every cervical cancer patient with curative intent for radiotherapy, treated at our department
Exclusion criteria
- Non-curative treatment
- Part of the treatment is given in another hospital
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Netherlands · 1 center
- University Medical Center Groningen — Groningen
Identifiers
NCT: NCT02733289 · 201600207