Menopause Clinical Trial
Official title:
Changes in the Hardness of Resilient Denture Liners Embedded in Maxillary Complete Dentures and Their Association With Patient Characteristics
Thirty complete maxillary denture wearers were recruited after obtaining informed consent.
One investigator measured the Shore D hardness of the commercially available RDLs using a
Vesmeter®. The salivary flow rates and pH values and the occlusal force were measured for
all patients before initiation of the study.
T-tests and Pearson's correlation coefficients were used for statistical analyses.
A p-value of <0.05 was considered statistically significant.
1. Participants This study was approved by the Human Ethics Committee of Nihon University
School of Dentistry, Matsudo (EC 13-006). Thirty wearers of complete maxillary dentures
(12 men; mean age, 71.8 ± 9.2 years and 18 women; mean age, 70.2 ± 10.7 years) who
visited the Department of Removable Prosthodontics at our institute were recruited for
this study. The volunteers were enrolled only after they provided written informed
consent. Complete maxillary denture wearers who had been treated with a tissue
conditioner, RDLs, and denture adhesives were excluded. Before starting the clinical
trial, the participants were asked about the following environmental factors in a
questionnaire: smoking, drinking, denture wearing during sleeping, and denture cleanser
usage.
After specimen making, all participants were instructed to wear their dentures as per
their normal routine.
2. Specimen Preparation A cylinder shapes six places with a 4-mm diameter and 2-mm depth ,
that was drilled into the inner surface of the denture base. Then, the RDL materials
were mixed by each product, packed into the cavity, and polymerized at room temperature
. The six commercial RDLs used in this study:Evatouch Super (EVA; Neo Dental Chemical
products, Washington, USA), GC RELINE (GCR; GC Dental Products Corp, Tokyo, Japan),
Mucopren soft (MCP; Kettenbach GmbH & Co KG, California, USA) Soften (SFT; KAMEMIZU
CHEM, Osaka, Japan), FD Soft (FDS; KAMEMIZU CHEM, Osaka, Japan), and Bio Liner (BIO;
Nissin Dental Products, Kyoto, Japan).
Hardness was measured using a Vesmeter® (WaveCyber Corp, Saitama, Japan). When the
probe, which included a built-in position sensor connected to a personal computer, was
placed in a perpendicular orientation to an RDL, the indenter of the probe was
depressed onto the RDL at a constant speed through electromagnetic power.
Simultaneously, the path of the indenter was constantly traced by the position sensor.
The computer processed electrical signals from the measuring device and calculated the
Shore D hardness, which was the primary outcome in the present study. The same
investigator measured the hardness at each appointment. The original hardness and the
hardness at 1 month after oral exposure were used for analysis. Each specimen was
measured five times, and the highest and lowest values were eliminated from the
calculation of the mean representative value for each specimen. The specimens embedded
in the dentures were measured on a hot plate to maintain the temperature at 37°C or as
close to the oral temperature as possible.
3. Statistical Analyses Before other statistical analyses, the normality of the data was
tested using the Kolmogorov - Smirnov test, and then parametric statistical methods
were applied.Two-way repeated measures analysis of variance ( ANOVA ) with the material
type (EVA, MCP, GCR, FDS, SFT, and BIO) and time period (baseline and one month after)
as factors was used to assess changes in the hardness of the six RDLs over time. The
Tukey-Kramer test was used as a post hoc test after the two-way repeated measures ANOVA
.The effects of categorical variables such as sex, smoking, drinking, denture wearing
during sleeping, and denture cleanser usage on the hardness of the RDLs were analyzed
using a two-way ANOVA without a post hoc test; we were not interested in comparing each
RDL but rather in analyzing the effects of categorical variables on the RDLs. The
effects of continuous variables, including age, salivary flow rate, and occlusal force,
were analyzed using Pearson's correlation coefficients. All statistical analyses were
performed using IBM® SPSS® Statistics 21 (IBM, Armonk, NY, USA). A p-value of <0.05 was
considered statistically significant.
;
N/A
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04553029 -
A Survey Evaluating Prevalence, Severity and Associated Factors in East Asian Women With Moderate-to-severe Menopause-related Vasomotor Symptoms (MR-VMS)
|
||
Completed |
NCT03672513 -
Short-term Supplementation, Bone Turnover and Antioxidant Status in Menopause
|
N/A | |
Terminated |
NCT03642119 -
Validation of an Objective Instrument to Measure Hot Flashes During Menopause
|
||
Completed |
NCT05387174 -
Nursing Intervention in Two Risk Factors of the Metabolic Syndrome and Quality of Life in the Climacteric Period
|
N/A | |
Completed |
NCT04210583 -
RF and PEMF for Treatment of Vaginal Laxity and Mons Pubis and Labia for Improvement of Skin Laxity
|
N/A | |
Completed |
NCT06057896 -
Effects of Combined Natural Molecules on Metabolic Syndrome in Menopausal Women
|
||
Completed |
NCT05617287 -
An Exploratory Investigation of Dietary Supplementation and the Effect on Common Symptoms of Perimenopause and Menopause
|
N/A | |
Recruiting |
NCT05180266 -
Therapeutic Touch and Music in The Menopausal Period
|
N/A | |
Recruiting |
NCT04043520 -
Bioenergetic Effects of Aging and Menopause (BEAM)
|
Phase 4 | |
Completed |
NCT03663075 -
Effect of Group Education and Individual Counselling on Mental Health and Quality of Life in 45-60 Year Old Women
|
N/A | |
Completed |
NCT03363997 -
Pharmacokinetics and Pharmacodynamics of 3 Dosages of Estriol After Continuous Vaginal Administration for 21 Days
|
Phase 1 | |
Not yet recruiting |
NCT04728126 -
Menopausal Symptoms and Burnout: Comparison of Occupational Health Issue Among Health Professionals in UMC Hospitals
|
||
Not yet recruiting |
NCT04724135 -
Assessment of Menopause Related Quality of Life Among Health Professionals in University Hospitals of UMC in Nur-Sultan
|
||
Completed |
NCT02274571 -
Raising Insulin Sensitivity in Post Menopause
|
Early Phase 1 | |
Completed |
NCT02430987 -
Low Sexual Desire and Metabolic Syndrome
|
N/A | |
Completed |
NCT02253173 -
Estradiol Vaginal Softgel Capsules in Treating Symptoms of Vulvar and Vaginal Atrophy in Postmenopausal Women
|
Phase 3 | |
Completed |
NCT01757340 -
Calorie Restriction With Leucine Supplementation
|
N/A | |
Recruiting |
NCT01488903 -
A Cohort Research of Genetic Susceptibility for Common Obesity in Women
|
N/A | |
Terminated |
NCT01633814 -
Hormone Replacement and Neural Cardiovascular Control in Postmenopausal Women
|
N/A | |
Completed |
NCT00599456 -
Investigation of the Usefulness of Omega 3 Vitamins in the Relief of Hot Flashes in Menopausal Women.
|
N/A |