Standard Follow-up Program Cervix Cancer (SFP CERVIX)

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02733289

Acronym

SFPCERVIX

Enrollment

10000

Registered

2016-04-11

Start date

2015-06-30

Completion date

2040-12-31

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Cancer Radiation Complications

Brief summary

Standard evaluation and follow-up data regarding complications of curative radiation treatment for cervical cancer.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
Complications	Five years	Physiological parameters, questionnaires

Countries

Netherlands

Contacts

Primary ContactJannet Beukema

j.c.beukema@umcg.nl+31503610025

Backup ContactPetra Veldhuijzen van Zanten

p.veldhuijzen@umcg.nl+31503614659

Outcome results