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Evaluation of the denture retention under the use of denture stability materials developed for patients with dry mouth.

Not yet recruiting
Conditions
Xerostomia
Registration Number
jRCT1032240582
Lead Sponsor
not applicable
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
26
Inclusion Criteria
  1. Patients who visit the Oral Function Management Department at Showa University Dental Hospital
  2. Patients who have had maxillary complete dentures made in our department and are undergoing regular checkups
  3. Individuals who have given written informed consent to participate in this study
Exclusion Criteria
  1. Those with oral mucositis or other abnormal findings.
  2. Persons who use drugs that affect salivary secretion on the day of measurement. (tricyclic and tetracyclic antidepressants, antihypertensive drugs such as loop diuretics and calcium channel blockers, antiparkinsonian drugs such as anticholinergics and L-dopa containing preparations).
  3. Persons who have experienced hypersensitivity symptoms due to the test sample.
  4. Persons who have difficulty swallowing.
  5. Persons who are deemed ineligible as research subjects by the investigator.

Study & Design

Study Type
Interventional
Study Design
crossover assignment
Primary Outcome Measures
NameTimeMethod
-

Retentive strength of duplicate denture after 30 minutes in each test sample

Secondary Outcome Measures
NameTimeMethod
Retentive strength of duplicate denture when test sample is not used

Retentive strength of duplicate denture when test sample is not used

Retentive strength of duplicate denture at 0, 10, and 20 minutes for each test sample0, 10, and 20 minutes

Retentive strength of duplicate denture at 0, 10, and 20 minutes for each test sample

Oral moistness

Oral moistness

Results of usability questionnaire (VAS values)

Results of usability questionnaire (VAS values)

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