MucoLock™ for Treatment of Stomatitis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBaptist Health South Florida
About this trial
The purpose of this research is to test how well people can tolerate MucoLock™ as a treatment for mouth pain or burning sensation and how well it works to reduce mouth pain or burning sensation. Study participants will be asked to use MucoLock™ topical solution as a "swish and spit" solution (similar to mouthwash) three times per day for 5 minutes each time, for 28 days.
Eligibility criteria
Qualifiers
Age 18 years and older
Individuals with oral dysesthesia (worst VAS sensitivity/burning score ≥ 7 over the last week)
Ability to understand and the willingness to sign a written informed consent document
Disqualifiers
Inability to comply with study instructions
Uncontrolled intercurrent illness or psychiatric illness/social situations that would limit compliance with study requirements*
Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the participant or the quality of the data.
Advanced kidney disease
Trial design
Treatments tested in this trial
- MucoLock Oral Gel
Treatment groups
25 Participants
are divided into 1 treatment groupSponsors and collaborators
Baptist Health South Florida
Lead sponsor
Professional Compounding Centers of America
Collaborator
Source ClinicalTrials.gov