Standard Follow-up Program Cervix Cancer (SFP CERVIX)

NCT ID: NCT02733289

Last Updated: 2024-02-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-06-30

Study Completion Date

2040-12-31

Brief Summary

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

Detailed Description

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Conditions

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Cervical Cancer Radiation Complications

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University Medical Center Groningen

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jannet Beukema

Role: PRINCIPAL_INVESTIGATOR

Principal Investigator

Locations

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University Medical Center Groningen

Groningen, , Netherlands

Site Status RECRUITING

Countries

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Netherlands

Central Contacts

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Jannet Beukema

Role: CONTACT

+31503610025

Petra Veldhuijzen van Zanten

Role: CONTACT

+31503614659

Facility Contacts

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Jannet Beukema

Role: primary

+31503610025

Other Identifiers

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201600207

Identifier Type: -

Identifier Source: org_study_id

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