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A single-center, open, randomized controlled clinical trial for Kangfuxin liquid combined with ice-throat 30-minute engraved sugar for prevention and treatment of acute oral mucositis caused by nasopharyngeal carcinoma

A single-center, open, randomized controlled clinical trial for Kangfuxin liquid combined with ice-throat 30-minute engraved sugar for prevention and treatment of acute oral mucositis caused by nasopharyngeal carcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018847
Enrollment
Unknown
Registered
2018-10-14
Start date
2018-10-20
Completion date
Unknown
Last updated
2018-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nasopharyngeal carcinoma

Interventions

Group 1:Given a Kangfuxin liquid combined with ice-throat 30-minute engraved sugar 30-minute
Control group:Compound tea polyphenols containing sputum.

Sponsors

Guizhou Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: (1) Voluntarily participate in the trial and sign an informed consent form; (2) Aged 18 to 69 years old male and female; (3) Patients with newly diagnosed nasopharyngeal carcinoma confirmed by histopathology and without distant metastasis; (4) 2017 AJCC 8th edition clinical stage of nasopharyngeal carcinoma is stage III-IVA. (5) It is scheduled to receive radical chemoradiotherapy (IMRT technology for radiotherapy and cisplatin for chemotherapy); (6) KPS = 70; (7) The estimated survival period is at least 6 months.

Exclusion criteria

Exclusion criteria: (1) active oral infectious diseases, including oropharyngeal candidiasis and facial herpes, or other oral diseases; (2) elderly patients with dry stomatitis; (3) patients with recurrent or residual nasopharyngeal carcinoma; (4) Combine severe heart, liver, kidney, hematopoietic and neurological diseases, psychiatric patients, and those who are not satisfied with glycemic control of diabetes; (5) Patients who are simultaneously using molecular targeted therapy; (6) Those who are allergic to the body, who are known or suspected to be allergic to the test drug; (7) pregnant women, lactating women, and women of childbearing age who cannot be effectively contraceptive during the trial; (8) Those who have participated in other drug clinical trials within 3 months; (9) Alcohol and/or drug abusers;There are other researchers who think that it is not suitable for this test.

Design outcomes

Primary

MeasureTime frame
Acute oral mucosal toxicity evaluation;Oral mucositis rating scale ulcer score;Pain rating;KPS score;

Secondary

MeasureTime frame
6/5000 Shengmìng zhìliàng cèdìng Quality of life measurement;

Countries

China

Contacts

Public ContactLi Yuanyuan

The Cancer Hospital of GuiZhou Province

lilyuanyuan@qq.com+86 188585899303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026