Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT07287826

Using a Steroid Mouthwash to Prevent Mouth Sores During Chemotherapy

Led by Woman's · Updated on 2026-03-30

45

Participants Needed

1

Research Sites

91 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if a steroid mouthwash (dexamethasone) can prevent mouth sores caused by chemotherapy in adults with cancer. The main questions it aims to answer are: Does using dexamethasone mouthwash before and during chemotherapy lower the chance of getting moderate to severe mouth sores? Can this approach reduce pain and improve comfort during chemotherapy? Researchers will compare patients using the mouthwash to a historical group of patients who received similar chemotherapy but did not use the mouthwash, to see if the mouthwash helps prevent mouth sores. Participants will: Use a steroid mouthwash (4 times daily) for up to 8 weeks during chemotherapy Complete a short weekly survey about mouth discomfort during infusion visits

CONDITIONS

Official Title

Using a Steroid Mouthwash to Prevent Mouth Sores During Chemotherapy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Confirmed cancer diagnosis
  • Scheduled to receive or currently receiving chemotherapy associated with oral mucositis (e.g., anthracyclines and taxanes)
  • Able to provide informed consent
  • Able to follow study procedures
Not Eligible

You will not qualify if you...

  • Current tobacco use or use within the past 6 weeks
  • HIV/AIDS diagnosis
  • Gastrointestinal disorders such as Crohn's disease, ulcerative colitis, or celiac disease
  • History of cold sores (herpes simplex virus)
  • Oral shingles (herpes zoster) within the past 6 weeks
  • Active oral infections at enrollment (e.g., candidiasis)
  • Known allergy or sensitivity to dexamethasone
  • Unable to self-administer or tolerate the mouthwash
  • Enrolled in conflicting clinical trials
  • Existing oral ulcers or mucositis at enrollment
  • Pregnant
  • Uncontrolled diabetes mellitus with HbA1c unknown or greater than 8% in the past 3 months despite therapy

AI-Screening

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Trial Site Locations

Total: 1 location

1

Woman's Hospital

Baton Rouge, Louisiana, United States, 70817

Actively Recruiting

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Research Team

J

Jaymes H Collins, PhD

CONTACT

E

Ericka Seidemann, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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