- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03256409
Bar and Ball Joint Overdentures Surface Roughness and Microbial Adherence
The aim of the study was to compare the surface roughness (Ra) of the implant retained mandibular bar overdenture (BOD) and the implant retained mandibular ball joint overdenture (BJOD) in jaw and its relation with the adhesion of molds and yeasts and mesophyll aerobe, in time 30 to 180 days in mouth. Five systems titanium bar CARES® and synOcta® Straumann® Dental Implant System, Holding AG Inc., Basel, Switzerland (BOD); and five systems joint ball Klockner® Implant System; Soadco Inc., Escaldes-Engordany; Andorra (BJOD), were used in two parallel groups of five participants, in an essay to simple blind person. To 30 to 180 days they were withdrawn and they were evaluated the Ra (Mitutoyo Surfest SJ-301® Mitutoyo Corporation Inc., Kanagawa, Japan) and the adhesion of microorganisms (CFU/ml).
The Ra:um (the 30th and 180th): BOD, 0.965 - 1.351; BJOD, 1.325 - 2.384. Adhesion: molds and yeasts, BOD, 2.6 x 102 and 4.6 x 103; BJOD, 3.0 x 102 and 5.3 x 104. Adhesion: mesophyll aerobe, BOD, 3.8 x 106 and 5.8 x 106; BJOD, 4.3 x 106 and 7.1 x 107. The BOD and BJOD, present different Ra (P < 0.05) to 30 to 180 days. To 30 days (P = 0.489) differences do not exist as regards the adhesion of molds and yeasts and mesophyll aerobe between both overdentures. To 180 days (P = 0.723) differences exist as regards the adhesion of mold and yeast and mesophyll aerobe, being major in BJOD.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Adherence mold and yeast and mesophyll aerobe to BOD and BJOD, Surface roughness (Ra), and Statistical Analyses Microbial populations have been controlled in the saliva at initial time and adherence at 30 to 180 days after the overdentures in the mouth. The saliva sample was obtained from the patient in a sterile sputum collection bottle through a sterile solution. The overdenture samples were extracted and processed for analysis. Each sample was submerged in ¼ sterile Ringer and subjected to vigorous ultrasound shaking. From each of the microbial suspensions, successive dilutions were made to determine the total number of viable microorganisms present. Total count of mold and yeast and total count of mesophyll aerobe were performed.
The surface roughness of BOD and BJOD was determined with the rugosimeter the Mitutoyo Surfest SJ-301® (Mitutoyo Corporation Inc., Kanagawa, Japan), through a displacement force of 4mN and of the tray to 0.5 mm/s and back to 1 mm/s (Murtra and Arcís,1999). The roughness profile Ra was evaluated and determined in microns (ųm) through five readings for each of the samples in the study respectively.
The results of BOD and BJOD were compared for the determination of Ra and the adherence of mold and yeast and mesophyll aerobe. For this, we used the statistics Shapiro-Wilk, T and the Pearson Correlation Coefficient to determinate the relationship between the study variables.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Total edentulous mandible from 50 to 60 years of age
- Absence of systemic conditions.
Exclusion Criteria:
- Hyperplasia and history of periodontal disease
- Patients with local and/or systemic antimicrobial treatment within 72 hours prior to evaluation during the study
- Signs of severe oral parafunction
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Five Bar overdenture: BOD
Five systems titanium bar CARES® and synOcta® Straumann® Dental Implant System, Holding AG Inc., Basel, Switzerland (Bar overdenture: Group 1) For the manufacture of the overdentures it was used as material of choice Lucitone 199® (Dentsply International Inc. York, PA) and for the adaptation of the retention systems it was used Softreliner Tough Soft® Tocuyama Dental Corporation Inc., Japan.
The working protocol for determining the BOD Ra and the adhesion of molds and yeasts and mesophyll aerobics was carried out entirely by an investigator.
Patients were randomly assigned to group 1.
The BOD were removed at 30 - 180 days for surface roughness evaluation (Ra:ųm) and the evaluation of the adhesion of mold and yeast and mesophyll aerobe (CFU/ml).
|
Adherence mold and yeast and mesophyll aerobe to BOD and BJOD Microbial populations have been controlled in the saliva at initial time and adherence at 30 - 180 days after the overdentures in the mouth.
The saliva sample was obtained from the patient in a sterile sputum collection bottle through a sterile solution.
The overdenture samples were extracted and processed for analysis.
Each sample was submerged in ¼ sterile Ringer and subjected to vigorous ultrasound shaking.
From each of the microbial suspensions, successive dilutions were made to determine the total number of viable microorganisms present.
Total count of mold and yeast and total count of mesophyll aerobe were performed.
Other Names:
The surface roughness of BOD and BJOD was determined with the rugosimeter the Mitutoyo Surfest SJ-301® (Mitutoyo Corporation Inc., Kanagawa, Japan), through a displacement force of 4mN and of the tray to 0.5 mm/s and back to 1 mm/s (Murtra and Arcís,1999).
The roughness profile Ra was evaluated and determined in microns (ųm) through five readings for each of the samples in the study respectively.
Other Names:
|
|
Experimental: Five Ball Joint Overdenture: BJOD
Five systems ball joint Klockner® Implant System; Soadco Inc., Escaldes-Engordany, Andorra (Ball Joint Overdenture: Group 2) For the manufacture of the overdentures it was used as material of choice Lucitone 199® (Dentsply International Inc. York, PA) and for the adaptation of the retention systems it was used Softreliner Tough Soft® Tocuyama Dental Corporation Inc., Japan.
The working protocol for determining the BJOD Ra and the adhesion of molds and yeasts and mesophyll aerobics was carried out entirely by an investigator.
Patients were randomly assigned to group 2. The s BJOD were removed at 30 - 180 days for surface roughness evaluation (Ra:ųm) and the evaluation of the adhesion of mold and yeast and mesophyll aerobe (CFU/ml).
|
Adherence mold and yeast and mesophyll aerobe to BOD and BJOD Microbial populations have been controlled in the saliva at initial time and adherence at 30 - 180 days after the overdentures in the mouth.
The saliva sample was obtained from the patient in a sterile sputum collection bottle through a sterile solution.
The overdenture samples were extracted and processed for analysis.
Each sample was submerged in ¼ sterile Ringer and subjected to vigorous ultrasound shaking.
From each of the microbial suspensions, successive dilutions were made to determine the total number of viable microorganisms present.
Total count of mold and yeast and total count of mesophyll aerobe were performed.
Other Names:
The surface roughness of BOD and BJOD was determined with the rugosimeter the Mitutoyo Surfest SJ-301® (Mitutoyo Corporation Inc., Kanagawa, Japan), through a displacement force of 4mN and of the tray to 0.5 mm/s and back to 1 mm/s (Murtra and Arcís,1999).
The roughness profile Ra was evaluated and determined in microns (ųm) through five readings for each of the samples in the study respectively.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Average values of surface roughness (Ra) and correlation of independent test in implant-retained mandibular bar overdentures (BOD) 30 - 180 days.
Time Frame: Change from 30 to 180 days
|
The average Ra Group 1: BOD titanium bar CARES® and synOcta Straumann® in 30 days: 0.965um.
In 180 days: 1.351um.
95% confidence and Shapiro Wilk (P > 0.05), determines normal distribution.
Correlation of independent test (P < 0.05) 30 days (P= 0.000) and 180 days (P=0.001)
determined different Ra.
Ll: Lower limit; Ul: Upper limit.
|
Change from 30 to 180 days
|
|
Average values of surface roughness (Ra) and correlation of independents tests in implant-retained ball joint overdentures (BJOD) 30 - 180 days.
Time Frame: Change from 30 to 180 days
|
The average Ra Group 2: BJOD Klockner® in 30 days: 1.325um.
180 days: 2.384 um.
95% confidence and Shapiro Wilk (P > 0.05), determines normal distribution.
Correlation of independent test (P < 0.05) 30 days (P=0.000) and 180 days (P=0.000)
determined different Ra.
Ll: Lower limit; Ul: Upper limit.
|
Change from 30 to 180 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Average values of mold and yeast adhesion and correlation of independents tests in implant-retained mandibular bar overdentures (BOD) and implant-retained mandibular ball joint overdentures (BJOD) 30 - 180 days
Time Frame: Change from 30 to 180 days
|
Average adhesion values of mold and yeast.
Group 1 (BOD): 30 days: 2.6 x 102 CFU/ml.
Group 2 (BJOD): 30 days: 3.0 x 102 CFU/ml.
Group 1 (BOD): 180 days: 4.6 x 103 CFU/ml.
Group 2 (BJOD): 180 days: 5.3 x 104 CFU/ml.
95% confidence and Shapiro Wilk (P > 0.05), determines normal distribution.
Correlation of independent tests 30 days (P > 0.05) BOD (P=0.051)
y BJOD (P=0.052)
showed no different adherence.
For 180 days (P < 0.05) BOD (P=0.025)
y BJOD (P=0.027)
presented different adhesion.
Ll: Lower limit; Ul: Upper limit
|
Change from 30 to 180 days
|
|
Average values of mesophyll aerobe adhesion and correlation of independents tests in implant-retained mandibular bar overdentures (BOD) and implant-retained mandibular ball joint overdentures (BJOD) 30 - 180 days
Time Frame: Change from 30 to 180 days
|
Average adhesion values of mesophyll aerobe.
Group 1 (BOD): 30 days: 3.8 x 106 CFU/ml.
Group 2 (BJOD): 30 days: 4.3 x 106 CFU/ml.
Group 1 (BOD): 180 days: 5.8 x 106 CFU/ml.
Group 2 (BJOD): 180 days: 7.1 x 107 CFU/ml.
95% confidence and Shapiro Wilk (P > 0.05), determines normal distribution.
Correlation of independent tests 30 days (P > 0.05) BOD (P=0.052)
y BJOD (P=0.053)
showed no different adherence.
For 180 days (P < 0.05) BOD (P=0.000)
y BJOD (P=0.000)
presented different adhesion.
Ll: Lower limit; Ul: Upper limit.
|
Change from 30 to 180 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rocío Violeta Valenzuela-Narváez, PhD DDS, CONCYTEC
Publications and helpful links
General Publications
- Stellingsma K, Slagter AP, Stegenga B, Raghoebar GM, Meijer HJ. Masticatory function in patients with an extremely resorbed mandible restored with mandibular implant-retained overdentures: comparison of three types of treatment protocols. J Oral Rehabil. 2005 Jun;32(6):403-10. doi: 10.1111/j.1365-2842.2005.01242.x.
- Portmann M, Glauser R. Report of a case receiving full-arch rehabilitation in both jaws using immediate implant loading protocols: a 1-year resonance frequency analysis follow-up. Clin Implant Dent Relat Res. 2006;8(1):25-31. doi: 10.2310/j.6480.2005.00027.x.
- Visser A, Meijer HJ, Raghoebar GM, Vissink A. Implant-retained mandibular overdentures versus conventional dentures: 10 years of care and aftercare. Int J Prosthodont. 2006 May-Jun;19(3):271-8.
- Degidi M, Piattelli A. Immediately loaded bar-connected implants with an anodized surface inserted in the anterior mandible in a patient treated with diphosphonates for osteoporosis: a case report with a 12-month follow-up. Clin Implant Dent Relat Res. 2003;5(4):269-72. doi: 10.1111/j.1708-8208.2003.tb00210.x.
- Elsyad MA, Ashmawy TM, Faramawy AG. The influence of resilient liner and clip attachments for bar-implant-retained mandibular overdentures on opposing maxillary ridge. A 5-year randomised clinical trial. J Oral Rehabil. 2014 Jan;41(1):69-77. doi: 10.1111/joor.12120. Epub 2013 Dec 20.
- van Kampen F, Cune M, van der Bilt A, Bosman F. Retention and postinsertion maintenance of bar-clip, ball and magnet attachments in mandibular implant overdenture treatment: an in vivo comparison after 3 months of function. Clin Oral Implants Res. 2003 Dec;14(6):720-6. doi: 10.1046/j.0905-7161.2003.00961.x.
- Lang R, Rosentritt M, Behr M, Handel G. Fracture resistance of PMMA and resin matrix composite-based interim FPD materials. Int J Prosthodont. 2003 Jul-Aug;16(4):381-4.
- Panyayong W, Oshida Y, Andres CJ, Barco TM, Brown DT, Hovijitra S. Reinforcement of acrylic resins for provisional fixed restorations. Part III: effects of addition of titania and zirconia mixtures on some mechanical and physical properties. Biomed Mater Eng. 2002;12(4):353-66.
- Uzun G, Keyf F. The effect of fiber reinforcement type and water storage on strength properties of a provisional fixed partial denture resin. J Biomater Appl. 2003 Apr;17(4):277-86. doi: 10.1177/0885328203017004003.
- Yap AU, Mah MK, Lye CP, Loh PL. Influence of dietary simulating solvents on the hardness of provisional restorative materials. Dent Mater. 2004 May;20(4):370-6. doi: 10.1016/j.dental.2003.06.001.
- Guler AU, Yilmaz F, Kulunk T, Guler E, Kurt S. Effects of different drinks on stainability of resin composite provisional restorative materials. J Prosthet Dent. 2005 Aug;94(2):118-24. doi: 10.1016/j.prosdent.2005.05.004.
- Bollen CM, Lambrechts P, Quirynen M. Comparison of surface roughness of oral hard materials to the threshold surface roughness for bacterial plaque retention: a review of the literature. Dent Mater. 1997 Jul;13(4):258-69. doi: 10.1016/s0109-5641(97)80038-3.
- Berger JC, Driscoll CF, Romberg E, Luo Q, Thompson G. Surface roughness of denture base acrylic resins after processing and after polishing. J Prosthodont. 2006 May-Jun;15(3):180-6. doi: 10.1111/j.1532-849X.2006.00098.x.
- Keyf F, Etikan I. Evaluation of gloss changes of two denture acrylic resin materials in four different beverages. Dent Mater. 2004 Mar;20(3):244-51. doi: 10.1016/S0109-5641(03)00099-X.
- Richmond R, Macfarlane TV, McCord JF. An evaluation of the surface changes in PMMA biomaterial formulations as a result of toothbrush/dentifrice abrasion. Dent Mater. 2004 Feb;20(2):124-32. doi: 10.1016/s0109-5641(03)00083-6.
- Mendonca MJ, Machado AL, Giampaolo ET, Pavarina AC, Vergani CE. Weight loss and surface roughness of hard chairside reline resins after toothbrushing: influence of postpolymerization treatments. Int J Prosthodont. 2006 May-Jun;19(3):281-7.
- Busscher HJ, van der Mei HC. Physico-chemical interactions in initial microbial adhesion and relevance for biofilm formation. Adv Dent Res. 1997 Apr;11(1):24-32. doi: 10.1177/08959374970110011301.
- Quirynen M, Bollen CM. The influence of surface roughness and surface-free energy on supra- and subgingival plaque formation in man. A review of the literature. J Clin Periodontol. 1995 Jan;22(1):1-14. doi: 10.1111/j.1600-051x.1995.tb01765.x.
- Radford DR, Challacombe SJ, Walter JD. Denture plaque and adherence of Candida albicans to denture-base materials in vivo and in vitro. Crit Rev Oral Biol Med. 1999;10(1):99-116. doi: 10.1177/10454411990100010501.
- Waltimo T, Tanner J, Vallittu P, Haapasalo M. Adherence of Candida albicans to the surface of polymethylmethacrylate--E glass fiber composite used in dentures. Int J Prosthodont. 1999 Jan-Feb;12(1):83-6.
- He XY, Meurman JH, Kari K, Rautemaa R, Samaranayake LP. In vitro adhesion of Candida species to denture base materials. Mycoses. 2006 Mar;49(2):80-4. doi: 10.1111/j.1439-0507.2006.01189.x.
- Yildirim MS, Hasanreisoglu U, Hasirci N, Sultan N. Adherence of Candida albicans to glow-discharge modified acrylic denture base polymers. J Oral Rehabil. 2005 Jul;32(7):518-25. doi: 10.1111/j.1365-2842.2005.01454.x.
- Daniluk T, Fiedoruk K, Sciepuk M, Zaremba ML, Rozkiewicz D, Cylwik-Rokicka D, Tokajuk G, Kedra BA, Anielska I, Stokowska W, Gorska M, Kedra BR. Aerobic bacteria in the oral cavity of patients with removable dentures. Adv Med Sci. 2006;51 Suppl 1:86-90.
- Busscher HJ, Uyen MH, van Pelt AW, Weerkamp AH, Arends J. Kinetics of adhesion of the oral bacterium Streptococcus sanguis CH3 to polymers with different surface free energies. Appl Environ Microbiol. 1986 May;51(5):910-4. doi: 10.1128/aem.51.5.910-914.1986.
- Pinna A, Zanetti S, Sechi LA, Carta F. In vitro adherence of Staphylococcus epidermidis, Serratia marcescens, and Pseudomonas aeruginosa to AcrySof intraocular lenses. J Cataract Refract Surg. 2005 Dec;31(12):2430-1. doi: 10.1016/j.jcrs.2005.08.049. No abstract available.
- Shimizu K, Kobayakawa S, Tsuji A, Tochikubo T. Biofilm formation on hydrophilic intraocular lens material. Curr Eye Res. 2006 Dec;31(12):989-97. doi: 10.1080/02713680601038816.
- Brusca MI, Chara O, Sterin-Borda L, Rosa AC. Influence of different orthodontic brackets on adherence of microorganisms in vitro. Angle Orthod. 2007 Mar;77(2):331-6. doi: 10.2319/0003-3219(2007)077[0331:IODOBO]2.0.CO;2.
- Ryan CS, Kleinberg I. Bacteria in human mouths involved in the production and utilization of hydrogen peroxide. Arch Oral Biol. 1995 Aug;40(8):753-63. doi: 10.1016/0003-9969(95)00029-o.
- Tada A, Watanabe T, Yokoe H, Hanada N, Tanzawa H. Oral bacteria influenced by the functional status of the elderly people and the type and quality of facilities for the bedridden. J Appl Microbiol. 2002;93(3):487-91. doi: 10.1046/j.1365-2672.2002.01702.x.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Gastrovital&Development
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Adhesiveness
-
Chattem, Inc.CompletedTolerability | Adhesiveness | Dermal Irritation | Effects of HeatUnited States
-
Chattem, Inc.CompletedTolerability | Adhesiveness | Dermal Irritation | Effects of HeatUnited States
Clinical Trials on Adherence mold and yeast and mesophyll aerobe
-
Charite University, Berlin, GermanyFriede Springer Stiftung, GermanyCompleted
-
Obstetrics & Gynecology Hospital of Fudan UniversityNot yet recruitingMayer Rokitansky Kuster Hauser Syndrome
-
Shanghai Zhongshan HospitalShanghai Changzheng HospitalRecruitingChronic Lymphocytic Leukemia Stage A(0) | Chronic Lymphocytic Leukemia Stage A(I) | Chronic Lymphocytic Leukemia Stage A(II) | Chronic Lymphocytic Leukaemia Stage B(I)China
-
Irccs SdnFederico II University; Fresystem S.p.A.Completed
-
Zhilei ShanNot yet recruitingElevated Blood Glucose
-
University of ParmaCompletedDietary ModificationItaly
-
National Cancer Institute (NCI)CompletedMycoses | Neutropenia | FeverUnited States
-
University of FloridaActive, not recruiting
-
Al-Azhar UniversityInnovinity medical hub; Smile trainNot yet recruitingUnilateral Cleft Lip | Nasoalveolar Molding
-
Huazhong University of Science and TechnologyNot yet recruitingPreDiabetes | Type 2 Diabetes