Evaluating Chinese Medicine Oral Rinse for Irradiated Oral Mucositis in Head & Neck Cancer Patients
NCT ID: NCT05664906
Last Updated: 2022-12-27
Study Results
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Basic Information
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UNKNOWN
PHASE1/PHASE2
40 participants
INTERVENTIONAL
2023-01-31
2024-11-30
Brief Summary
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Detailed Description
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The risk of OM is especially high in NPC patients who receive concomitant chemotherapy, receive a total dose over 5,000 Gy, treat with altered fractionation radiation schedules, have bad oral hygiene status, do not use antibiotic at early stage mucositis, have smoking history, drink alcohol, have problems in nutritional status like anorexia, malnutrition, lack of vitamins, restriction of food due to specific dietary requirements, have haematological disease or non-ideal hematological status, have advanced localization of tumors and stage, receive immunotherapy, have pre-existing dry mouth (Xerostomia), have episodes of OM during prior treatment cycles and low BMI, etc.
According to some weighed guidelines such as The Multinational Association of Supportive Care in Cancer and International Society for Oral Oncology (MASCC/ISOO) guidelines for the management of OM, recent systematic reviews and researches, there are mainly several sections for intervention: (1) Basic oral care, (2) Anti-inflammatory agents, (3) Photobiomodulation, (4) Cryotherapy, (5) Antimicrobials, coating agents, anesthetics, and analgesics, (6) Growth factors and cytokines, and (7) Natural and miscellaneous. We can summarize several suggestions for the prevention of OM in H\&N cancer adults receiving RT from the above protocols: multiagent combination oral care protocols (increasing the awareness of good oral hygiene), professional dental care (a desirable option before or during cancer therapy for local and systemic infections from odontogenic sources), benzydamine mouthwash (as the anti-inflammaotary agents for moderate dose of RT (\<50 Gy)) and intraoral photobiomodulation therapy using low-level laser therapy. Over the years, the number of interventions studied for OM and their quality of study design have been dramatically increasing. However, since there are still some advantages and disadvantages for some suggested agents, some clinical settings have not yet been recommended with appropriate intervention. Natural and miscellaneous agents are also reviewed in the past years while honey is suggested for prevention of OM in patients with H\&N cancer who receive treatment with either RT or chemo-RT. However, if honey is applied repeatedly on a daily basis for a longer period, we have to be cautions with its deleterious effects. A strict oral hygiene protocol has to be followed to prevent dental caries.
For the Chinese Medicine (CM) interventions, many studies have been reviewed on the efficacy of mouthwash or internal herbal decoction to OM. Although some positive results were observed, most of them were performed by applying different assessment tools and lack of quality of life (QOL) or self-reported symptoms assessment. In addition, the intervention time and follow-up period were usually insufficient (stopped at the end of RT), therefore they could not review the long-term efficacy of CM according to normal progression of OM and the safety of using CM. Therefore, we hope this pilot study can evaluate the efficacy and safety of CM in a strict protocol.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Intervention Group: Chinese Medicine Oral Rinse and Standard Care
* Prescription and oral rinsing with Chinese Medicine Oral Rinse Formula-I (CMORF-I) which mainly consists of the Nong's concentrated CM granules of Wu Wei Xiao Du Yin and other ingredients.
* Standard care will be following the indications provided by patient's western medical doctor.
* Patients should not take any other TCM and non-prescribed medication and nutritional supplements during the intervention period.
Chinese Medicine Oral Rinse Formula-I (CMORF-I)
* Prescription of Chinese Medicine Oral Rinse Formula-I (CMORF-I)
* Instruction to rinse:
1. The above amount of concentrated CM granules will be divided and packed in 4 bags per day.
2. Dissolve 1 bag of concentrated CM granules with 150ml 80'C boiled hot water, and wait for 20 mins to cool down.
3. Clean the mouth thoughtfully by rinsing with 150ml of distilled water for 2 minutes.
4. Rinse the mouth thoughtfully with one-third of the dissolved and cooled CM oral rinse, gargle, expel after 3 minutes, do not swallow and repeat twice.
5. To ensure better contact of the CM oral rinse in all parts and folds of the oral cavity, our research assistant and CMP will guide the patients to fully agitate the mouth, use the tongue to stir repeatedly among the teeth, cheeks and palate surface, and to raise the tip of the tongue for a moment and tilt the head back.
6. 4 times a day (half an hour after every meal, half an hour before sleep), from baseline to 2 weeks after RT.
Standard Care
• Standard care including normal saline or medical mouthwash, optional analgesics and antibiotics will be offered by hospital.
Control Group: Placebo and Standard Care
* Placebo: The placebo consists of an inert substance, made of starch filler, flavor and colorings. It is also manufactured under GMP standard. To ensure blinding, the CMORF-I formula and placebo will be indistinguishable in appearance, smell and favour.
* Standard care will be following the indications provided by patient's western medical doctor.
* Patients should not take any other TCM and non-prescribed medication and nutritional supplements during the intervention period.
Standard Care
• Standard care including normal saline or medical mouthwash, optional analgesics and antibiotics will be offered by hospital.
Placebo
Placebo granules, instruction is the same as CMORF-I.
Interventions
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Chinese Medicine Oral Rinse Formula-I (CMORF-I)
* Prescription of Chinese Medicine Oral Rinse Formula-I (CMORF-I)
* Instruction to rinse:
1. The above amount of concentrated CM granules will be divided and packed in 4 bags per day.
2. Dissolve 1 bag of concentrated CM granules with 150ml 80'C boiled hot water, and wait for 20 mins to cool down.
3. Clean the mouth thoughtfully by rinsing with 150ml of distilled water for 2 minutes.
4. Rinse the mouth thoughtfully with one-third of the dissolved and cooled CM oral rinse, gargle, expel after 3 minutes, do not swallow and repeat twice.
5. To ensure better contact of the CM oral rinse in all parts and folds of the oral cavity, our research assistant and CMP will guide the patients to fully agitate the mouth, use the tongue to stir repeatedly among the teeth, cheeks and palate surface, and to raise the tip of the tongue for a moment and tilt the head back.
6. 4 times a day (half an hour after every meal, half an hour before sleep), from baseline to 2 weeks after RT.
Standard Care
• Standard care including normal saline or medical mouthwash, optional analgesics and antibiotics will be offered by hospital.
Placebo
Placebo granules, instruction is the same as CMORF-I.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* are the first time to receive RT to the primary tumor in the area of the head or face, neck, or oral cavity.
* start RT recently within 14 days.
* are assessed by CMPs for the condition of oral mucositis according to modified World Health Organization (WHO) Mucositis Grades with Grade ≦1.
* have Karnofsky Performance Status (KPS) ≥ 60 (patients require occasional assistance, but is able to care for most personal needs will be 60 or above).
* are able to read or understand and sign the consent form.
Exclusion Criteria
* have known medication on bacterial or fungal infections of oropharynx at recruitment.
* have other known diseases such as serious and uncontrolled Diabetes mellitus (with symptom of delayed wound healing over the past half year) or hyperthyroidism (with symptom of serious oral dryness over the past half year), known connective vascular disorders or known Human Immunodeficiency Virus (HIV) infections etc.
* have known history of allergy to CMORF-I ingredients or Glucose-6-Phosphate Dehydrogenase (G6PD) patients.
* are known pregnant or breastfeeding.
18 Years
ALL
No
Sponsors
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Chinese University of Hong Kong
OTHER
Responsible Party
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Au Kwok Yin
Dr. AU Kwok Yin
Principal Investigators
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KWOK YIN AU, Doctor of Medicine
Role: PRINCIPAL_INVESTIGATOR
Hong Kong Institute of Integrative Medicine
Locations
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Hong Kong Institute of Integrative Medicine
Hong Kong, , Hong Kong
Countries
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Central Contacts
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Facility Contacts
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KWOK YIN AU, PhD
Role: primary
References
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Other Identifiers
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CM Rinse_OMRT
Identifier Type: -
Identifier Source: org_study_id