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Effects for Oral Mucositis Care During Chemoradiotherapy in Cancer Patients: Evaluation of the Bee Products

Prevention and Improvement for Oral Mucositis Care During Chemoradiotherapy in Head and Neck Cancer Patients With Honey Production

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05625841
Acronym
Mucositis
Enrollment
135
Registered
2022-11-23
Start date
2022-11-25
Completion date
2024-12-31
Last updated
2022-11-23

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

Conditions

Oral Mucositis

Keywords

Oral Mucositis

Brief summary

Oral mucositis is common among cancer patients receiving radiotherapy and chemotherapy. 80-90% of the patients are suffering from the mucositis pain; poor nutrition and even treatment discontinued. Some self-paid medications like glutamine has been used to prevent mucositis before and during radiotherapy/chemotherapy. Randomized controlled trials have shown that honey and propolis may be used for the management of mucositis. Honey demonstrates the most significant antibacterial effects; the green propolis has also been proved to comprise antibacterial, anti-inflammatory, and antioxidant effects. Bee products have been concerned as potential sources of natural antioxidants such as flavonoids, phenolic acids, and terpenoids. This study plan to conduct an RCT comparing the effectiveness of honey, honey and green propolis, and usual care in mucositis of cancer patients.

Detailed description

Outcome Measures 1. Questionnaire collection: oral mucositis grade, pain scale, fatigue scale, dry mouth, nutritional status and quality of life scale. 2. Wearing the smart bracelet: The smart bracelet will automatically detect heart rate variability, heartbeat, sleep and activity status. 3. Saliva sample collection: Test the concentration of IL-1, IL-6, IL-10 and TNF in saliva. 4. Stool and oral flora collection: Test stool and oral flora microbiota.

Interventions

OTHERHoney product

Bee products intervention from the first day of radiation to the end of radiation therapy duration 8-12 weeks.

OTHERpropolis

propolis

OTHERUsual care

Usual care

Sponsors

Taipei Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. diagnosed with a head and neck tumor. 2. receive chemotherapy or radiotherapy. 3. conscious clear and willing to participate in the research. 4. can communicate in Mandarin or Taiwanese.

Exclusion criteria

diabetes, arrhythmia, artificial heart rhythm device, allergic to bee products or alcohol.

Design outcomes

Primary

MeasureTime frameDescription
oral mucositis severityup to 12 weeksUlceration or inflammation of the oral mucosa characterizes oral Mucositis

Secondary

MeasureTime frameDescription
fatigue levelup to 12 weeksBrief Fatigue Inventory
Xerostomia scoreup to 12 weeksXerostomia Inventory
nutrition levelup to 12 weeksMini Nutritional Assessment
pain scoreup to 12 weeksvisual analogue score(VAS)
smart bracelet dataThe first week, the fourth week, the 8th week start wearing the smart bracelet for 7 daysThe smart bracelet will automatically detect heart rate variability, heartbeat, sleep and activity status
Saliva specimen collectionThis saliva is collected Baseline (before the start of radiotherapy), week 1, week 2, week 3, and up to 12 weeksTest the concentration of IL-1, IL-6, IL-10 and TNF in saliva
microbiota levelBaseline (Before the start of radiotherapy), week 2, week 4, and up to 12 weeksStool and oral flora collection
QoL questionnaireup to 12 weeksFACT-HN

Countries

Taiwan

Contacts

Primary ContactTsai-Wei Huang, PhD
tsaiwei@tmu.edu.tw886-2-2736-1661
Backup ContactTsai-Wei Huang, PhD

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026