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Comparison of the Effects of Oral Ulceration Healing in Patients Wearing a Removable Denture

NCT06531720 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2024-08-01

No results posted yet for this study

Summary

The aim of the study was comparing the effectiveness of oral mucosa healing properties of different preparations: CHX=0,2% chorhexidine digluconate, CHS=8,7% choline salicylate, CON=control group, in patients with delivered removable dentures, during the adaptation period.

Conditions

  • Oral Mucosa; Ulcer

Interventions

DRUG

Chlorhexidine Gluconate

topical preparation applied on oral mucosa lesion containing 0,2% CHX

DRUG

Choline Salicylate 8.7 % Oral Gel

topical preparation applied on oral mucosa lesion containing, ethanol-based

OTHER

control group

no medication has been prescribed

Sponsors & Collaborators

  • Medical University of Silesia

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06531720 on ClinicalTrials.gov