Evaluation of complications from radiation treatment for cervical cancer
Standard Follow-up Program Cervix Cancer (SFP CERVIX)
This study is looking at the side effects and recovery experiences of women with cervical cancer who are receiving radiation treatment to see how it affects them over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Sex | Female |
| Sponsor | University Medical Center Groningen Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Groningen) |
| Trial ID | NCT02733289 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather standard follow-up data on complications experienced by patients undergoing curative radiation treatment for cervical cancer. It involves evaluating the outcomes and side effects of the treatment over time. The study will include all cervical cancer patients treated with curative intent at the University Medical Center Groningen, focusing on their recovery and any complications that arise post-treatment.
Who should consider this trial
Good fit: Ideal candidates for this study are cervical cancer patients who are receiving curative radiation treatment.
Not a fit: Patients undergoing non-curative treatment or those receiving part of their treatment at another hospital may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the understanding of radiation-related complications, leading to better management and care for cervical cancer patients.
How similar studies have performed: While this study focuses on standard follow-up, similar observational studies have shown success in understanding treatment complications in other cancer types.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Groningen
- University Medical Center Groningen — Groningen, Netherlands (Recruiting)
Study contacts
- Principal investigator: Jannet Beukema — Principal Investigator
- Study coordinator: Jannet Beukema
- Email: j.c.beukema@umcg.nl
- Phone: +31503610025
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.