Clinical trial · Interventional
Taurine for the Prevention and Treatment of Radiation-induced Oral Mucositis in Patients With Nasopharyngeal Carcinoma
Taurine for the Prevention and Treatment of Radiation-induced Oral Mucositis in Patients With Nasopharyngeal Carcinoma: a Single-center, Open-label, Randomized Phase 2 Clinical Trial
NCT07567742CI-TRIAL-00110395not yet recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This clinical trial aims to understand whether taurine can prevent and reduce severe radiation-induced oral mucositis in patients with nasopharyngeal carcinoma undergoing radiotherapy.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Nasopharyngeal Carcinoma (NPC) | Nasopharyngeal Carcinoma | ONTOLOGY_EXACT | 0.85 |
| Oral Mucositis (Ulcerative) Due to Radiation | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Taurine | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Taurine
- description
- Oral taurine 1 g twice daily, starting 3 days before radiotherapy until 1 week after completion of radiotherapy, plus standard of care for RIOM.
- interventionNames
- Drug: Taurine
- type
- NO_INTERVENTION
- label
- Control
- description
- Patients in the control arm will receive the standard of care for RIOM.
Primary outcomes (1)
- measure
- Incidence of Severe Radiation-Induced Oral Mucositis
- timeFrame
- From the start of radiotherapy to 4 weeks after completion of radiotherapy
- description
- The incidence of Grade ≥3 radiation-induced oral mucositis (RIOM) in the experimental and control groups, as assessed using the Radiation Therapy Oncology Group (RTOG) acute RIOM grading scale.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age 18-70 years. 2. Histologically confirmed newly diagnosed non-keratinizing nasopharyngeal carcinoma (WHO classification). 3. Non-metastatic nasopharyngeal carcinoma (Stage I-III) according to the AJCC 9th edition staging system. 4. Scheduled to receive radical intensity-modulated radiotherapy (IMRT). 5. No prior history of anti-cancer treatment. 6. ECOG performance status 0-1; adequate organ function within 2 weeks before enrollment; Hematology: hemoglobin \> 90 g/L; absolute neutrophil count \> 1.5×10⁹/L; platelet count \> 100×10⁹/L. Biochemistry: total bilirubin ≤ 1.5×ULN; ALT, AST ≤ 2.5×ULN; ALP ≤ 2.5×ULN; creatinine clearance ≥ 50 mL/min. 7. For patients with abnormal ECG or prior cardiovascular disease, additional cardiac function tests and echocardiography must be normal. 8. Provided written informed consent and willing to comply with study visits, treatment, laboratory tests, and other protocol requirements. Exclusion Criteria: 1. Known intolerance or hypersensitivity to taurine or its excipients. 2. Conditions that interfere with oral drug administration (e.g., dysphagia, chronic diarrhea, intestinal obstruction). 3. Prior history of malignant tumor. 4. Pregnant or lactating women. (Pregnancy testing is required for women of childbearing potential; effective contraception must be used during treatment.) 5. History or presence of severe oral ulcers, oral diseases, or salivary gland diseases. 6. Unwilling to stop smoking, drinking alcohol, or chewing betel nut. 7. Presence of severe active comorbidities. 8. Severe dysfunction of heart, brain, lung, or other vital organs. 9. Active infection requiring treatment; long-term use of immunosuppressive agents; psychiatric disorders. 10. Unable to complete radiotherapy or likely to delay radiotherapy for more than 1 week due to subjective factors. 11. Any other condition deemed inappropriate by the investigator.
References
Publications (0)
Data not yet available
No reference posted for this study.