Radiation Induced Oral Mucositis Clinical Trial
Official title:
Efficacy and Safety of Lappaconitine Adhesive Patch for the Treatment of Oral Mucositis Pain Caused by Chemoradiotherapy in Patients With Nasopharyngeal Cancer ： A Randomized, Prospective Single-center Controlled Study
The purpose of this clinical study is to evaluate the efficacy of lappaconitine adhesive patch in alleviation radiation induced mucositis pain and the improvements in QOL of patients with nasopharyngeal carcinoma . To determine if lappaconitine administered prior to radiation therapy reduces the severity of radiation induced oral mucositis pain in patients who have been diagnosed with nasopharyngeal carcinoma.
This is a randomized, single -center study conducted in China to evaluate Lappaconitine
Adhesive Patch in the reduction severity of radiation induced oral mucositis pain in patients
receiving solo radiation therapy or chemoradiation therapy for nasopharyngeal carcinoma.
Patients will reveive daily fractions of IMRT (2.0 - 2.2 Gy) to a total of 60 - 72 Gy over
approximately 7 weeks, plus cisplatin administered 80 - 100 mg/m2 once every three weeks for
3 doses or 30 - 40 mg/m2 once weekly for 6-7 doses (investigator's choice).
Patients in both arms received Intensity Modulated Radiation Therapy(IMRT) :All target
volumes were outlined slice by slice on the axial contrast-enhanced CT with MR fusion images
in the treatment planning system. The target volumes were defined in accordance with the
International Commission on Radiation Units and Measurements Reports 50 and 62. The
prescribed dose is 68-72 Gy to PTVnx (Planning target volume of the primary tumor), 64-68 Gy
to GTVnd (Gross tumor volume of the cervical lymph node), 60- 64Gy to PTVnd and PTV1
(Planning target volume 1), and 54-58 Gy to PTV2 (Planning target volume 2) in 30-32
fractions.
Patients will be randomized equally to 1 of 2 treatment arms:
Arm A: Lappaconitine Adhesive Patch per day, concurrent with stardard care for oral mucositis
Arm B: stardard care for oral mucositis
All patients will be assessed weekly for oral mucositis per WHO grading criteria until the
completion of IMRT, and once weekly thereafter (if necessary) for 7 weeks, or until oral
mucositis resolves to ≤ Grade 1.
Approximately 200 patients will be enrolled to ensure that roughly 80 patients per arm
complete treatments for primary endpoint analysis.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT02508389 -
A Study of the Effects of GC4419 on Radiation Induced Oral Mucositis in Patients With Head/Neck Cancer
|
Phase 2 | |
| Not yet recruiting |
NCT04292990 -
Comparison of Transdermal Fentanyl and Morphine for Oral Mucositis Pain in Nasopharyngeal Cancer Patients
|
Phase 4 |