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Recruiting NCT02435576

NCT02435576 Standard Follow-up Program (SFP) for Head and Neck Cancer Patients

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Clinical Trial Summary
NCT ID NCT02435576
Status Recruiting
Phase
Sponsor University Medical Center Groningen
Condition Head and Neck Cancer
Study Type OBSERVATIONAL
Enrollment 10,000 participants
Start Date 2007-03
Primary Completion 2025-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Radiotherapy (primary or postoperative)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 10,000 participants in total. It began in 2007-03 with a primary completion date of 2025-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary and general objective of the clinical introduction of the SFP as the current standard of care is to improve the quality of radiotherapy for head and neck cancer patients by reducing radiation-induced side effects without hampering treatment efficacy in terms of locoregional tumour control and overall survival and to systematically evaluate the beneficial effect of newly introduced radiation technology for this particular group of patients. The clinical introduction of the SFP will allow for a systematic and broad scale quality improvement cycle for head and neck cancer patients treated with radiotherapy. In fact, this methodology can be considered a kind of quality circle for the clinical introduction of new radiation techniques, aiming at continuous efforts for further improvement.

Eligibility Criteria

Inclusion Criteria: * All patients planned for curatively intended primary or postoperative radiotherapy will be included. At the first visit, patients are informed about the standard follow up program by the treating physician. Exclusion Criteria: * All patients planned for palliative radiotherapy will not be included in the SFP.

Contact & Investigator

Central Contact

J.A. Langendijk, Prof. Dr.

✉ j.a.langendijk@umcg.nl

📞 +31503615532

Principal Investigator

J.A. Langendijk, Prof. Dr.

PRINCIPAL INVESTIGATOR

University Medical Center Groningen

Frequently Asked Questions

Who can join the NCT02435576 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Head and Neck Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT02435576 currently recruiting?

Yes, NCT02435576 is actively recruiting participants. Contact the research team at j.a.langendijk@umcg.nl for enrollment information.

Where is the NCT02435576 trial being conducted?

This trial is being conducted at Groningen, Netherlands.

Who is sponsoring the NCT02435576 clinical trial?

NCT02435576 is sponsored by University Medical Center Groningen. The principal investigator is J.A. Langendijk, Prof. Dr. at University Medical Center Groningen. The trial plans to enroll 10,000 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology