Magic Mouthwash Plus Sucralfate Versus Benzydamine Hydrochloride for the Treatment of Radiation-induced Mucositis

Sponsor
Juravinski Cancer Centre Foundation (Other)
Overall Status
Completed
CT.gov ID
NCT00814359
Collaborator
(none)
67
1
2
16
4.2

Study Details

Study Description

Brief Summary

Radiation treatment is very effective for treating cancers of the head and neck, however, during the course of treatment, it is common for patients to experience soreness of their mouth and throat due to the radiation. When radiation causes inflammation of the inside of the mouth, it is called 'mucositis'. There are several mouthwashes that are commonly used to prevent and treat mucositis, but none of these have been shown to be superior to another. This study is being conducted to see if using a combination of magic mouthwash and sucralfate is better than using a single mouthwash called benzydamine at decreasing the burden of mucositis.

Condition or Disease Intervention/Treatment Phase
  • Drug: Combination of Magic Mouthwash Plus Sucralfate
  • Drug: 0.15% Benzydamine HCl
Phase 3

Detailed Description

Sixty patients with head and neck cancer being treated with 6 or more weeks of radiotherapy, will be randomly assigned to receive either a combination of magic mouthwash (diphenhydramine, dexamethasone and nystatin) plus sucralfate or benzydamine. Patients randomized to receive magic mouthwash plus sucralfate will rinse first with 5ml of the magic mouthwash for 2 minutes then swallow, followed by rinsing with 5ml of the 1g/5ml sucralfate for 2 minutes before swallowing, 4 times daily. Patients randomized to receive 0.15% benzydamine HCl will be instructed to rinse with 15ml of the solution for 2 minutes before expectorating, 4 times daily. Patients will start the mouthwash regimens prior to the initiation of radiotherapy, and stop 2 weeks after the completion of radiotherapy.

Study Design

Study Type:
Interventional
Actual Enrollment :
67 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
A Phase III Study of Magic Mouthwash Plus Sucralfate Versus Benzydamine HCl for Treatment of Radiation-induced Oral Mucositis in Head and Neck Cancer Patients.
Study Start Date :
May 1, 2009
Actual Primary Completion Date :
Sep 1, 2010
Actual Study Completion Date :
Sep 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: Magic Mouthwash Plus Sucralfate

Drug: Combination of Magic Mouthwash Plus Sucralfate
Magic mouthwash will contain diphenhydramine powder 375mg, dexamethasone injection 2.8mg, and nystatin suspension 50ml (1000 units/ml) diluted to a total volume of 250ml with sterile water. The concentration of the sucralfate suspension will be 1g/5ml. Patients will be instructed to rinse first with 5ml of the magic mouthwash solution for 2 minutes then swallow, followed by rinsing with 5ml of the sucralfate suspension for 2 minutes before swallowing, repeating this 4 times daily, starting on the day prior to the initiation of radiotherapy, and stopping 2 weeks after the completion of radiotherapy.
Other Names:
  • Mucositis Mouthwash
  • Sulcrate
  • Active Comparator: Benzydamine HCl

    Drug: 0.15% Benzydamine HCl
    Patients will rinse with 15ml of 1.5mg/ml benzydamine HCl for 2 minutes then expectorate the solution, repeating this 4 times daily, starting on the day prior to the initiation of radiotherapy, and stopping 2 weeks after the completion of radiotherapy.
    Other Names:
  • Tantum
  • Outcome Measures

    Primary Outcome Measures

    1. The severity of patient-reported symptoms of mucositis as determined by the change in Oral Mucositis Weekly Questionnaire - Head and Neck Cancer (OMWQ-HN) score from baseline to 6 weeks. [Baseline to 6 weeks after the initiation of radiotherapy.]

    Secondary Outcome Measures

    1. The severity of patient-reported symptoms of mucositis throughout the course radiotherapy as determined by the area under the curve for mean change in OMWQ-HN scores from baseline. [Baseline to 10 weeks after initiating radiotherapy.]

    2. Incidence of WHO Grade 3 or 4 oral mucositis after 4 weeks of radiotherapy. [4 weeks after initiating radiotherapy]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Histologically proven squamous cell carcinoma of the head and neck.

    • Receiving 6 or more weeks of external beam radiotherapy to a treatment volume that includes mucosal surfaces of the head and neck.

    Exclusion Criteria:
    • Age less than 18 years

    • ECOG Performance Score 2 or higher

    • Patient is unable to understand the protocol and/or unable to provide informed consent

    • Patient is unable or unwilling to complete the questionnaires which are written in English.

    • Prior radiation to the head and neck region that would result in overlap of fields for the current study.

    • Plan to receive a radiation treatment volume that only includes the larynx and or hypopharynx with no planned treatment of locoregional lymph nodes.

    • Plan to receive a concurrent chemotherapy agent other than cisplatin.

    • Plan to receive other investigational agents (eg. panitumumab).

    • Investigational agent of any kind within 30 days prior to randomization.

    • Concurrent administration of any other experimental intervention given for the purpose of preventing oral mucositis.

    • History of allergic or hypersensitivity reactions to any of the possible agents to be administered in the study.

    • Patients who are pregnant or lactating.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Juravinski Cancer Centre Hamilton Ontario Canada L8V 5C2

    Sponsors and Collaborators

    • Juravinski Cancer Centre Foundation

    Investigators

    • Principal Investigator: Joda Kuk, MD, Juravinski Cancer Centre

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00814359
    Other Study ID Numbers:
    • MUCOSA-PROTECT
    First Posted:
    Dec 24, 2008
    Last Update Posted:
    Jan 20, 2011
    Last Verified:
    May 1, 2009

    Study Results

    No Results Posted as of Jan 20, 2011