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Recruiting Phase 3 NCT06241612

NCT06241612 Individualized Elective Neck Irradiation in NPC Patients

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Clinical Trial Summary
NCT ID NCT06241612
Status Recruiting
Phase Phase 3
Sponsor Sun Yat-sen University
Condition Nasopharyngeal Carcinoma
Study Type INTERVENTIONAL
Enrollment 470 participants
Start Date 2024-04-16
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Individualized Elective Neck Irradiation

Eligibility Fast-Check

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

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 3 trials are large pivotal studies comparing the treatment to current standard of care or placebo. Your participation directly contributes to the evidence needed for regulatory approval.

This trial targets 470 participants in total. It began in 2024-04-16 with a primary completion date of 2026-12-31.

⚠ 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

To evaluate whether individualized elective neck irradiation for nasopharyngeal carcinoma based on the vertebral level of metastatic lymph nodes can reduce the incidence of radiation-related adverse effects and improve patients' quality of life,without reducing survival.

Eligibility Criteria

Inclusion Criteria: * The eligibility criteria are: newly diagnosed, untreated, non-distant metastatic, and non-keratinizing NPC; nodes are diagnosed with PET/CT and MRI; staged as T1-4N0-2 or N3 category of non-bilateral lower-neck node metastasis; aged between 18 and 70 years; Karnofsky performance-status score \> 70; adequate haematological function, with a leucocyte count \> 4 × 109/L, haemoglobin \> 90 g/L, and a thrombocyte count \> 100×109/L Exclusion Criteria: * The exclusion criteria include: previous chemotherapy treatment, surgery (except diagnostic) or radiotherapy to the neck or nasopharyngeal regions; previous malignancy; lactation or pregnancy; or severe coexisting illness.

Contact & Investigator

Central Contact

Ling-Long Tang, Prof

✉ tangll@sysucc.org.cn

📞 02087343840

Frequently Asked Questions

Who can join the NCT06241612 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Nasopharyngeal Carcinoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06241612 trial and what does that mean for participants?

Phase 3 trials are large-scale studies comparing the new treatment to existing standards of care or a placebo. They provide the evidence needed for regulatory approval. This trial targets 470 participants.

Is NCT06241612 currently recruiting?

Yes, NCT06241612 is actively recruiting participants. Contact the research team at tangll@sysucc.org.cn for enrollment information.

Where is the NCT06241612 trial being conducted?

This trial is being conducted at Guangzhou, China.

Who is sponsoring the NCT06241612 clinical trial?

NCT06241612 is sponsored by Sun Yat-sen University. The trial plans to enroll 470 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