Topical Chlorhexidine Spray for the Prevention of Acute Radiation Dermatitis in Patients With Nasopharyngeal Carcinoma:
Recruiting now · Phase 3
Conditions studied: Nasopharangeal Cancer
In brief
This study investigated the effects of topical chlorhexidine spray on the incidence, severity, and quality of life during radiotherapy in nasopharyngeal carcinoma patients.
Key facts
- Study ID
- NCT07559877
- Run by
- Jiangxi Provincial Cancer Hospital
- People needed
- 148
- Starts
- 2026-04-01
- Expected to finish
- 2027-09-30
- Last updated by the study team
- 2026-04-30
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologically or cytologically confirmed nasopharyngeal carcinoma. Clinical stage II-III disease with N≥1, according to the UICC/AJCC 9th edition. Planned to receive first-course definitive chemoradiotherapy, with a total radiotherapy dose of 60-70 Gy.
- Able to communicate and complete study assessments. Willing to participate and able to provide written informed consent. Eligible based on baseline assessments performed before chemoradiotherapy.
You may not qualify if…
- History of or current psychiatric disorder, cognitive impairment, or other severe organic disease.
- Presence of another concomitant malignancy. Receipt of any other prophylactic intervention for radiation dermatitis. Pre-existing skin disease before chemoradiotherapy. Known hypersensitivity or allergy to chlorhexidine.
Where it is running
- Jiangxi Cancer Hospital — Nanchang, Jiangxi, China (enrolling)
Full record on ClinicalTrials.gov
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