New radiation approach aims to reduce dry mouth in throat cancer patients
NCT ID NCT04528394
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two types of radiation therapy for nasopharyngeal cancer (a cancer in the upper throat). One group received standard photon radiation plus carbon ion therapy, and the other received proton radiation plus carbon ion therapy. The main goal was to see which approach causes less severe dry mouth, a common side effect. The trial enrolled 136 adults with newly diagnosed cancer and compared side effects and tumor control between the two groups.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Radiation therapy (proton or photon combined with carbon ion)
- What this could lead to
- If it works, this could show that proton therapy causes less dry mouth than standard photon therapy for people with nasopharyngeal cancer.
- What could go wrong
- This is a small, early-phase trial (136 people) that only compares two types of radiation. It may not prove which is better overall, and results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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136 people
The number who actually took part.
- Started
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Apr 2019
- Finished
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Jun 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pathologically confirmed Nasopharyngeal carcinoma(WHO II/III type). * Age ≥ 18 and ≤ 70 years of age. * Eastern Cooperative Oncology Group score: 0-1. * Adequate laboratory values within 30 dyas of enrollment to study defined as follows: 1) neutrophil \> 2000/mm\^3; 2) platelet \> 100,000/mm\^3; 3) total bilirubin \< 1.5mg/dl; 4) alanine aminotransferase/aspartate aminotransferase \< 1.5 upper limit of normal; 5) SCr \< 1.5mg/dl; creatinine clearance rate \> 60ml/min. * Willing to accept adequate contraception for women with childbearing potential. * Willing to sign the written informed consent; Informed consent must be signed before the enrollment in the trial. Exclusion Criteria: * Presence of distant metastasis. * Received radiotherapy for head and neck before. * Received surgery(except for biopsy) for primary lesion or cervical lymph node. * Previous history of malignant tumor (within 5 years) or simultaneous existence of multiple primary tumors. * Presence of diseases (such as Sjögren syndrome) that may interfere evaluation of xerostomia. * Accompanied with severe major organ dysfunction. * Presence of mental disease that may influence the understanding of informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Shanghai Proton and Heavy Ion Center
Shanghai, Shanghai Municipality, 201315, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Could adding extra chemo before standard therapy beat nasopharyngeal cancer?
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