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AdhesionPhase 2/3NCT02434601

Dentin Treatments for Restorations of Cervical Lesions Non-Carious

A Phase 2/3 study testing Treatment of Dentin Surface, Dentin Surface and Treatment in people with Adhesion, run by Federal University of Pelotas.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The surface of non-carious cervical lesions (LCNC) is a challenge to adhesive systems, it presents a dentin layer sclera hypermineralized, presence of bacteria and lack of mechanical retention, so this study aimed to evaluate the influence of different surface treatments on LCNC through a randomized clinical trial. Read more about this study

Who is it for?
Ages 13 years and olderHealthy volunteers can take part
Conditions the study is for
Adhesion
What is being tested?
Treatment of Dentin Surface, Dentin Surface and Treatment
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
28 participants
Where
No sites listed yet
Study dates
Mar 2011to Oct 2016
Phase
Phase 2/3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 13 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Presence of at least three non-carious cervical lesions on the buccal aspect of previous vital teeth or premolars;
  • Visible plaque index presence and / or gingival bleeding index of at most 20%;
  • Probing depth of at least 3 mm in the experimental site and / or buccal 4 mm in any place;
  • Patients with good general health condition;
  • Patients able to understand and sign the letter of information and the free and informed consent;
  • Patients willing to return every six months to revaluation queries.

Who cannot join

  • Presence of less than 20 teeth in the mouth;
  • Patients undergoing orthodontic treatment;
  • Patients with occlusion problems;
  • Veneers with wear over 50% of the incisal / occlusal structure;
  • Absence of tooth antagonist.

About this study

Official title: Dentin Treatments for Restorations of Cervical Lesions Non-carious: a Randomized Clinical Trial of Three Years

The surface of non-carious cervical lesions (LCNC) is a challenge to adhesive systems, it presents a dentin layer sclera hypermineralized, presence of bacteria and lack of mechanical retention, so this study aimed to evaluate the influence of different surface treatments on LCNC through a randomized clinical trial. Patients with LCNC were referred to the study and selected according to the inclusion criteria, such as the presence of at least 3 LCNC. Three different types of surface treatment were carried out in LCNC: control group, 15 seconds of etching dentin; Group I, acid etching of dentin in 30 seconds; and group II, cavity prophylaxis with ultrasound for 30 seconds. The remaining steps of the adhesive and restorative procedure was the same for all groups, following the material manufacturer's recommendations. Evaluations of restorations will be carried out in periods of one week (baseline), six months, one year, two years and three years as of tooth sensitivity, integrity and color change. Data will be analyzed by McNemar and chi-square test.

Read the detailed description

Ethical considerations This study was designed and conducted according to the guidelines Consolidated Standards of Reporting of Trials (CONSORT) for the preparation of randomized controlled clinical trials (Altman et al., 2001), after approval by the Research Ethics Committee (protocol number CEP-035 -2011- FO / UFPel), Faculty of Dentistry, Federal University of Pelotas - RS / Brazil.

Study design

Calculation for determining the sample

Based on the literature, the sample size was obtained assuming an average annual rate of failure 6% for Class V restorations performed with conventional adhesive systems (PEUMANS et al., 2005b), with 80% power and significance level of 5%. From the recommendations of the American Dental Association (2010), we estimated an annual failure rate of 12% for restorations in relative isolation. For this, a sample of 28 was determined by monitoring patients for a minimum of 5 years, considering possible attrition of 20%.

Recruitment and selection of patients The search strategy of individuals interested in participating in this clinical trial was conducted through the dissemination of the project through the display of posters and distribution of pamphlets in FO / UFPEL as well as in basic health units (BHU) located in the urban area Pelotas. In addition, the study had the collaboration of students representatives of class associations, coordinating teachers of clinical activities and dentists the public health system, to increase the receptivity and the accession of potential volunteers.

All patients were referred, or directly sought dental care, with diagnosis of non-carious cervical lesion, were scheduled for evaluation exam.

Two students of the seventh semester, under the supervision of the responsible of this study, carried out the consultations on the premises of FO / UFPEL. Initially, the presence of LCNC was assessed by visual inspection with wooden spatula aid. If so, we filled out a patient's medical record, containing identification data, general and dental history. In addition, the dental chart was performed using mirror, explorer, millimeter periodontal probe, clinical tweezers, cotton rolls and saliva sucker. From the clinical examination, the LCNC were sorted review of its features. The dentin sensitivity was evaluated by applying air jet for 3 seconds, the distance 2-3 cm of the labial surface, and sensitivity degree record from a visual analogue scale. Likewise, the pulpal vitality was visualized using cotton balls previously moistened with the gas jet cooling at -50 ° C.

Patients who met the inclusion and exclusion criteria received an information letter about the nature and proposal of the study. After reading, we asked the volunteers to sign a consent form and informed about their participation.

In a second clinic session, the patients underwent a process of adaptation of oral health for the prevention, control, removal of plaque and dental calculus. Professional intervention consisted in scraping, smoothing and polishing dental, using curettes / periodontal files, glass / rubber cone, Robinson brush, prophylaxis paste and contra angle low speed.

Operator training Six candidates for operators (students between the seventh and eighth semester of FOUFPEL) participated in a training process to ensure the standardization of clinical procedures and minimize the variation of different operators.

First stage (theoretical): A lecture was given, lasting about two hours, consisting in the presentation of materials and techniques for the removal or modification of hypermineralized surface layer of dentin-carious cervical lesions. It was also performed routine detailed statement to be instituted during the sessions. A manual containing the material operating instructions and the protocol of clinical procedures, was made available to students.

Second stage (practice): Students went through pre-clinical activities, watching the demonstration and subsequently performing Class V restorations on mannequins. Secondly, they performed the same procedures for volunteers who, despite presenting LCNC with restorative needs, were not included in this study. Therefore, such patients received restorative treatment under conditions identical to the patients involved in the study, but not part of the sample.

At the end of training and calibration steps, the functions of the working group delegated by using the performance of individual students as selection criteria. Were chosen two operators, who have restorative procedures, and two assistants to support operators and completion of medical records. The other students were in charge of sterilization of instruments, scheduling appointments, molding, photographic record, oral hygiene orientation, periodontal treatment, among other dental procedures offered to patients. All the above mentioned steps were performed under direct supervision of the responsible for the study.

Preparation of the patient: Four weeks before the start of the study, the patients were subjected to a sweep session, smoothing and polishing supragingival. In addition, patients received individualized instruction for mechanical control of dental biofilm, including guidance on the brushing technique and flossing. During the monitoring period, was also offered dental support to patients involved in the study.

Clinical Protocol Initially, prophylaxis element to be restored was made with glass and rubber based slurry of pumice and water. Then the color of the restoration was selected with the aid of a color scale (Vitapan Classical, Vita Zahnfabrik, Bad Säckingen, Germany). Local anesthesia was Also, when necessary. In the same query, the patient received restorative action in three LCNC to submit clinical features compatible. Randomization as the technique for the surface layer removal or modification hypermineralized to be applied in each place by drawing lots. The restorations were initiated by the previous LCNC, with the priority needs, the main complaint: aesthetic, functional aspects and / or symptoms such as tooth sensitivity, etc. Each patient had to have at least 3 teeth to be restored because of the 3 types of treatments employed. It draw lots 3 treatments individually for each tooth. For example, if a patient possessed the three lesions selected, the drawing is performed to be selected for each tooth treatment be subjected to a treatment. If the patient possess more than 3 lesions was performed again for the draw element 4 and so on with the other.

We emphasize also that each operator held the same number of restorative interventions, and one was prepared following the protocol recommended by the manufacturer of the materials, another increasing the etching time to 30 seconds on dentin and finally the third cavity was restored after performing a cavity prophylaxis with ultrasound probe applied for 30 seconds. The remaining steps were carried out following the protocol recommended by the manufacturer of restorative materials employed.

The rubber dam was accomplished through the use of lip retractor, wire retractor # 000 (Ultrapak Cord, Ultradent, South Jordam, UT, USA), cotton rolls and saliva sucker. The first element to be introduced in the oral cavity was the lip retractor, printing expulsion lips and cheeks. Cotton rolls were positioned in the upper labial sulcus at the lower labial sulcus and in the sublingual region, to absorb the saliva flow coming mainly from the major salivary glands. The retractor wire is inserted into the gingival sulcus with the aid of blunt spatula, without generating excessive pressure in the periodontium.

Prior to the implementation of restoration, there has been no type of cavity preparation, or beveling of cavosurface margins. However, each LCNC dentin surface was subjected to various removal or modification of the techniques hypermineralized ultra-surface layer, as follows:

  • Control Group: Restoration made following the protocol recommended by the manufacturer of the materials;
  • Experimental Group 1: Increase the etching time to 30 seconds, performed with phosphoric acid gel at 37%, prior to application of the resin adhesive. The following steps to acid etching followed the protocol recommended by the manufacturer of the materials;
  • Experimental Group 2: Prophylaxis cavity with ultrasound probe, applied for 30 seconds on the dentin surface hypermineralized of cervical lesions non-carious. Soon after, the restoration was made following the protocol recommended by the manufacturer of the materials.

Both restorative procedures were performed using a conventional adhesive system (Single Bond II, 3M ESPE, St. Paul, MN, USA) and composite restorative nanoparticulate (Filtek Z350, 3M ESPE, St. Paul, MN, USA), closely following the operating instructions provided by the manufacturer. The restorations were placed by incremental technique using about 2 or 3 increments restorative composite, as the size of LCNC. The increments were taken and adapted to the cavity starting with the margin in enamel with spatulas, brushes and siliconadas tips for composite resin. An LED device with minimum intensity 1450 mW / cm2 was used for polymerization.

Finally, the finish of the restoration was performed by using # 12 scalpel blade, diamond and fine-grained multi-laminated drills, in order to remove excess material and / or improve the shape of the contour restorations. The polishing of the same was done with employment siliconadas tips, floppies sandpaper (Sof-Lex Pop-On, 3M ESPE, St. Paul, MN, USA), felt-specific folders and polishing discs.

Reviews of restorations Two examiners (graduated in Dentistry) will go through a training process and calibration until present intra agreement index and inter-examiner of at least 80%. In the event of disagreement as to the assessment criteria, the same terião to get a consensus through direct revaluation of restorations and / or by means of digital photographs.

After the training phase and calibration, the evaluators 'blind', ie without any involvement with the conditions which patients will be submitted, shall proceed independently, clinical evaluations of restorations. At this time, the evaluators will use magnifying glass, mirror, explorer, millimeter periodontal probe, clinical tweezers, cotton rolls and saliva sucker. Data relating to dentin sensitivity and pulp vitality will also be collected through the air jet application and application cotton balls have been wetted with gas jet cooling to -50 ° C, respectively. Digital photographs will also be consulted by the evaluators.

The properties will be evaluated sensitivity, color change and integrity of the restoration.

Statistical analysis Clinical evaluations will occur in the following periods: 1 week (baseline), six months, a year, two years and three years after insertion of the restorations using the evaluated criteria. The data will be tabulated and submitted to statistical analysis, considering 80% power and 5% significance level.

Will be held descriptive analysis with calculation of ratios to characterize the sample and dental restorations. To compare outcomes in the pre- and post-intervention according to the treatment groups and also the comparison of outcome between treatment groups will be used chi-square test and McNemar test. The analyzes will be performed using Stata 12.1 software.

Conditions
Adhesion
Being tested
Treatment of Dentin Surface, Dentin Surface, Treatment
Keywords
Non-carious cervical lesions, Randomized clinical trial, Permanent dental restoration, Dentin, Adhesion, Restoration, Sensitivity, Prophylaxis, Randomized
Medical subject headings
Tissue Adhesions, Hypersensitivity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Treatment of Dentin SurfaceProcedure or surgery

    Also called Preconditioning of Dental Surface

    • Experimental Group 1: Increase the etching time to 30 seconds, performed with phosphoric acid gel at 37%, prior to application of the resin adhesive.
    • Experimental Group 2: Prophylaxis cavity probe / blunt tip of ultrasound, applied for 30 seconds on the dentin surface hypermineralized of cervical lesions non-carious.

    Both restorative procedures were performed using a conventional adhesive system and composite restorative nanoparticulate.

  • Dentin SurfaceProcedure or surgery

    Treatment of Dentin Surface: Increased etching dentin for 15 seconds to 30 seconds

  • TreatmentProcedure or surgery

    Treatment of Dentin Surface: Intervention with the cavity prophylaxis probe ultrasound blunt applied for 30 seconds in Surface hypermineralized non-carious dentin cervical lesions. Therefore, the restoration was done following the protocol recommended by the manufacturer of the material.

Study groups in NCT02434601
Study groupRoleWhat they receive
Treatment of Dentin SurfaceOtherTreatment of Dentin Surface: Restoration made following the protocol recommended by the manufacturer of the materials.
Receives: Procedure: Treatment of Dentin Surface
Dentin SurfaceExperimentalTreatment of Dentin Surface: Increased etching dentin for 15 seconds to 30 seconds
Receives: Procedure: Dentin Surface
TreatmentExperimentalTreatment of Dentin Surface: Intervention with the cavity prophylaxis probe ultrasound blunt applied for 30 seconds in Surface hypermineralized non-carious dentin cervical lesions. Therefore, the restoration was done following the protocol recommended by the manufacturer of the material.
Receives: Procedure: Treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of teeth with lost restorations

    Measured: From Baseline restorations at 3 years

Secondary outcomes (2)
  1. Presence or not of marginal leakage

    Measured: From Baseline restorations at 3 years

  2. Presence or not of dentin hypersensitivity

    Measured: From Baseline restorations at 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 May 2015 (estimated)
  2. Study startMar 2011
  3. Primary completionMar 2013
  4. Study completionOct 2016 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
28 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02434601
Sponsor's protocol ID
Federal University of Pelotas
Status last verified
Apr 2015
First submitted
4 Mar 2015
Last updated
5 May 2015
Results posted
No
Data monitoring committee
Yes

Publications

  • Demarco FF, Baldissera RA, Madruga FC, Simoes RC, Lund RG, Correa MB, Cenci MS. Anterior composite restorations in clinical practice: findings from a survey with general dental practitioners. J Appl Oral Sci. 2013 Nov-Dec;21(6):497-504. doi: 10.1590/1679-775720130013.

    PubMed 24473714
  • Akimoto N, Takamizu M, Momoi Y. 10-year clinical evaluation of a self-etching adhesive system. Oper Dent. 2007 Jan-Feb;32(1):3-10. doi: 10.2341/06-46.

    PubMed 17288322
  • Bartlett D, Ganss C, Lussi A. Basic Erosive Wear Examination (BEWE): a new scoring system for scientific and clinical needs. Clin Oral Investig. 2008 Mar;12 Suppl 1(Suppl 1):S65-8. doi: 10.1007/s00784-007-0181-5. Epub 2008 Jan 29.

    PubMed 18228057
  • Bartlett DW, Lussi A, West NX, Bouchard P, Sanz M, Bourgeois D. Prevalence of tooth wear on buccal and lingual surfaces and possible risk factors in young European adults. J Dent. 2013 Nov;41(11):1007-13. doi: 10.1016/j.jdent.2013.08.018. Epub 2013 Sep 1.

    PubMed 24004965
  • Hickel R, Roulet JF, Bayne S, Heintze SD, Mjor IA, Peters M, Rousson V, Randall R, Schmalz G, Tyas M, Vanherle G. Recommendations for conducting controlled clinical studies of dental restorative materials. Clin Oral Investig. 2007 Mar;11(1):5-33. doi: 10.1007/s00784-006-0095-7. Epub 2007 Jan 30.

    PubMed 17262225
  • Karakaya S, Unlu N, Say EC, Ozer F, Soyman M, Tagami J. Bond strengths of three different dentin adhesive systems to sclerotic dentin. Dent Mater J. 2008 May;27(3):471-9. doi: 10.4012/dmj.27.471.

    PubMed 18717178
  • Kim SY, Lee KW, Seong SR, Lee MA, Lee IB, Son HH, Kim HY, Oh MH, Cho BH. Two-year clinical effectiveness of adhesives and retention form on resin composite restorations of non-carious cervical lesions. Oper Dent. 2009 Sep-Oct;34(5):507-15. doi: 10.2341/08-006C.

    PubMed 19830963
  • Lopes GC, Baratieri CM, Baratieri LN, Monteiro S Jr, Cardoso Vieira LC. Bonding to cervical sclerotic dentin: effect of acid etching time. J Adhes Dent. 2004 Spring;6(1):19-23.

    PubMed 15119583
  • Lopes GC, Vieira LC, Monteiro S Jr, Caldeira de Andrada MA, Baratieri CM. Dentin bonding: effect of degree of mineralization and acid etching time. Oper Dent. 2003 Jul-Aug;28(4):429-39.

    PubMed 12877429
  • Moretto SG, Russo EM, Carvalho RC, De Munck J, Van Landuyt K, Peumans M, Van Meerbeek B, Cardoso MV. 3-year clinical effectiveness of one-step adhesives in non-carious cervical lesions. J Dent. 2013 Aug;41(8):675-82. doi: 10.1016/j.jdent.2013.05.016. Epub 2013 Jun 6.

    PubMed 23747824
  • Perdigao J. Dentin bonding-variables related to the clinical situation and the substrate treatment. Dent Mater. 2010 Feb;26(2):e24-37. doi: 10.1016/j.dental.2009.11.149. Epub 2009 Dec 14.

    PubMed 20005565
  • Peumans M, Kanumilli P, De Munck J, Van Landuyt K, Lambrechts P, Van Meerbeek B. Clinical effectiveness of contemporary adhesives: a systematic review of current clinical trials. Dent Mater. 2005 Sep;21(9):864-81. doi: 10.1016/j.dental.2005.02.003.

    PubMed 16009415
  • Ritter AV, Heymann HO, Swift EJ Jr, Sturdevant JR, Wilder AD Jr. Clinical evaluation of an all-in-one adhesive in non-carious cervical lesions with different degrees of dentin sclerosis. Oper Dent. 2008 Jul-Aug;33(4):370-8. doi: 10.2341/07-128.

    PubMed 18666493
  • Da Rosa Rodolpho PA, Donassollo TA, Cenci MS, Loguercio AD, Moraes RR, Bronkhorst EM, Opdam NJ, Demarco FF. 22-Year clinical evaluation of the performance of two posterior composites with different filler characteristics. Dent Mater. 2011 Oct;27(10):955-63. doi: 10.1016/j.dental.2011.06.001. Epub 2011 Jul 16.

    PubMed 21762980
  • Salz U, Bock T. Testing adhesion of direct restoratives to dental hard tissue - a review. J Adhes Dent. 2010 Oct;12(5):343-71. doi: 10.3290/j.jad.a19741.

    PubMed 20978636

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing Treatment of Dentin Surface, Dentin Surface and Treatment in people with Adhesion, run by Federal University of Pelotas.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 5 May 2015. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of teeth with lost restorations (time frame: From Baseline restorations at 3 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02434601, which also lists 17 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2015; AzTrials last refreshed its copy on 7 Nov 2026.

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