Evaluation the Effects of Herbal Gargle for Chemoradiotherapy-induced Oral Mucositis of Head & Neck Cancer, a Pilot Study.

Chang Gung Medical Foundation

Status and phase: Not yet enrolling; Phase 2

Conditions: Stomatitis and Ulceration; Chemoradiotherapy; Head and Neck Neoplasms

Treatments: Drug: Herbal gargle; Other: Normal saline

Study type: Interventional

Funder types: Other

Identifiers

NCT05341206

202101017A3

Details and patient eligibility

About

The aim of the study is to evaluate the effects of Herbal gargle on chemoradiotherapy-induced stomatitis in head & neck cancer patients.

Full description

Head and neck cancer accounts for about 5% of all cancers worldwide with the age-standardized incidence rate (ASIR) of HNC increased by 5.4% per year among males and 3.1% among females in Taiwan. Concurrent chemoradiotherapy (CCRT) is the most common management to treat head and neck cancer. However, CCRT may cause much side effects such as oral mucositis, radiation dermatitis, xerostomia, or infection, which influence food intake, disturb nutritional status and interrupt the course of treatment. Traditional Chinese Medicine (TCM) has been applied to treat cancer side effects for many years. Herbal gargle is composed of TCM herbals used for oral mucositis induced by chemoradiotherapy among head and neck cancer. The aim of the trial is to evaluate the effectiveness of Herbal gargle. The participants divide into two groups, treatment group and control group. The treatment group receive Herbal gargle 150ml and are instructed to hold the gargle in the mouth for 30s and then expectorate it twice a day, 5 days a week for 8 weeks. The control group receive normal saline 150ml for oral mucositis. The subjective questionnaires of EORTC QLQ-C30, EORTC QLQ-H&N35 are assessed twice a week, CTCAE for grading of oral mucositis is assessed once a week, VAS is assessed everyday for 8 weeks. Besides, change of opioid dosage, body weight are also recorded. The CRP is assessed before and every week for 8 weeks and the albumin and bacteria culture are assessed before and post-treatment of 4th week and 8th week. The baseline difference of treatment and control group will be analyzed by using independent t-test and the difference of evaluation scores and blood tests between pre-treatment and post-treatment will be analyzed using multivariate logistic regression analysis. A value of P < 0.05 will be regarded as statistically significant for the above statistical analyses.

Enrollment: 80 estimated patients

Sex: All

Ages: 20+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Willing to join the trial project and sign the informed consent form.
• Age more than 20 years-old.
• Pathology proved to be head and neck cancers.
• Head and neck cancer patients under radiotherapy or concurrent chemoradiotherapy.
• Expected life expectancy more than 3 months.
• Subjects with clear consciousness and can be assessed cooperatively.
• Subjects are suitable to use Herbal gargle evaluated by Traditional Chinese medicine physicians.

Exclusion criteria

• Subjects can not sing the informed consent form.
• Systemic infection.
• Heart, liver and kidney insufficiency
• Allergy history of Traditional Chinese medicine
• Unclear conscious to use Herbal gargle.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

80 participants in 2 patient groups

Treatment group

Experimental group

Description:

The treatment group receive Herbal gargle 150ml and are instructed to hold the gargle in the mouth for 30s and then expectorate it twice a day, 5 days a week for 8 weeks.

Treatment:

Drug: Herbal gargle

Control group

Sham Comparator group

Description:

The control group receive Normal saline 150ml and are instructed to hold the normal saline in the mouth for 30s and then expectorate it twice a day, 5 days a week for 8 weeks.

Treatment:

Other: Normal saline