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European Study on Three Different Approaches to Managing Class 2 Cavities in Primary Teeth

Primary Purpose

Dental Caries

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Hall Technique
Non-Restorative Caries Treatment
Conventional Restoration
Sponsored by
University Medicine Greifswald
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dental Caries focused on measuring Class II carious primary molar, Non-Restorative Caries Treatment, Hall Technique, Conventional restorations, Children

Eligibility Criteria

3 Years - 8 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

- Children aged 3-8 years who attend the Preventive and Paediatric Department of Greifswald University, Germany.

(Lithuania: children who attend the paediatric dentistry department, Dental Faculty, Lithuanian University of Health Sciences)

  • At least one primary molar tooth with caries into dentine involving two dental surfaces (diagnosed according to the International Caries Detection and Assessment System [ICDAS], codes 3 to 5)
  • Willing to be examined

Exclusion Criteria:

  • Clinical or radiographic signs of pulpal or peri-radicular pathology
  • Patients with a systemic disease requiring special considerations during their dental treatment.
  • Parents/children who refuse to participate in the study

Sites / Locations

  • Ernst-Moritz-Arndt-Universität Greifswald. Dental Faculty, Preventive and Paediatric Dentistry Department
  • Lithuanian University of Health Sciences, Dental Faculty, Clinic of Dental and Oral Pathology
  • University of Dundee, Dentistry & Nursing , College of Medicine, Unit of Dental and Oral Health School of Dentistry

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Hall Technique

Non-Restorative Caries Treatment

Conventional Restoration

Arm Description

This technique uses preformed Stainless Steel Crowns (SSCs) to restore carious primary molars. Local anaesthesia, caries removal or tooth preparation are not required.

This is a less operative approach, here carious lesions are opened removing the overhanging enamel and making the cavity accessible for biofilm removal. No carious dentine will be removed from the pulpal wall and no local anaesthesia will be placed. Fluoride varnish (Duraphat ®) will be applied to the cavity. Parents/children will be trained to clean the cavity by brushing using a buccolingual technique.

This technique corresponds to the conventional way of treating cavitated carious lesions involving complete caries removal, use of local anaesthesia (when needed), and a compomer (Dyract ®) restoration. Cotton wool roll isolation and continuous aspiration will be used.

Outcomes

Primary Outcome Measures

Failure Rate of the Three Treatment Arms Judged Clinically
Failure rate of the three treatment arms judged clinically after 2 years such as clear caries progression, secondary caries, loss of restoration, reversible pulpitis treated without requiring pulpotomy

Secondary Outcome Measures

Number of Children Experiencing Irreversible Pulpitis, Dental Abscess, or Extraction
Number of children experiencing irreversible pulpitis, dental abscess, or extraction judged clinically after 2 years

Full Information

First Posted
February 20, 2013
Last Updated
August 9, 2022
Sponsor
University Medicine Greifswald
Collaborators
University of Dundee, Lithuanian University of Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT01797458
Brief Title
European Study on Three Different Approaches to Managing Class 2 Cavities in Primary Teeth
Official Title
Randomised Control Trial on Three Different Approaches to Managing Class 2 Cavities in Primary Teeth
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medicine Greifswald
Collaborators
University of Dundee, Lithuanian University of Health Sciences

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this randomized clinical trial is to compare the clinical effectiveness of three treatments involving different caries management strategies (conventional restorations, Hall technique, and Non-Restorative Caries Treatment) to the management of class II carious primary molars in children (3-8 year-old).
Detailed Description
At present, many materials and techniques are used to treat carious primary teeth. All of these have their proponents who claim they provide the best performance in terms of longevity, aesthetics, bio-compatibility, etc (Qvist, 2010; Yengopal et al., 2009). However, despite the great variety of techniques and materials, there is no definite evidence for the most effective approach when dental caries in primary molars is concerned, as yet. On the other hand, there is conclusive evidence that shows that glass-ionomer cement is an inappropriate material for class II restorations in primary teeth, due to its significant shorter longevity compared with other restorative materials like compomer and amalgam. Recently, there is re-surging interest in more biological (less-invasive) techniques: such as the Non-Restorative Caries Treatment (Peretz & Gluck, 2006; Gruythuysen et al., 2010) or stainless steel crowns with the advent of the Hall technique in Scotland (Innes et al., 2007). However, there is lack of comparative evidence from high quality clinical trials leading to uncertainty in the effectiveness of these techniques. In addition, these techniques are rarely compared with standard fillings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries
Keywords
Class II carious primary molar, Non-Restorative Caries Treatment, Hall Technique, Conventional restorations, Children

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
169 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hall Technique
Arm Type
Experimental
Arm Description
This technique uses preformed Stainless Steel Crowns (SSCs) to restore carious primary molars. Local anaesthesia, caries removal or tooth preparation are not required.
Arm Title
Non-Restorative Caries Treatment
Arm Type
Experimental
Arm Description
This is a less operative approach, here carious lesions are opened removing the overhanging enamel and making the cavity accessible for biofilm removal. No carious dentine will be removed from the pulpal wall and no local anaesthesia will be placed. Fluoride varnish (Duraphat ®) will be applied to the cavity. Parents/children will be trained to clean the cavity by brushing using a buccolingual technique.
Arm Title
Conventional Restoration
Arm Type
Active Comparator
Arm Description
This technique corresponds to the conventional way of treating cavitated carious lesions involving complete caries removal, use of local anaesthesia (when needed), and a compomer (Dyract ®) restoration. Cotton wool roll isolation and continuous aspiration will be used.
Intervention Type
Procedure
Intervention Name(s)
Hall Technique
Intervention Description
Technique: Removal of dental plaque and rest of aliments from the cavity Selection of the SSC If the contact points are very tight, orthodontic separator elastics could be placed through the mesial and distal contacts and the SSC has to be fitted at a subsequent appointment Dry the crown and fill with glass-ionomer luting cement Place the crown over the tooth Removal of cement excesses from the crown margins The child should be asked to keep biting on the crown until the cement has set
Intervention Type
Procedure
Intervention Name(s)
Non-Restorative Caries Treatment
Intervention Description
Technique: A high-speed bur should be used to remove the undermined enamel and make the cavity accessible for plaque removal. Do not remove the contact area Clean, dry the cavity and apply Duraphat® varnish fluoride (50/mg/ml) Show the cavity to patient/parents and give them tooth-brushing instructions Tell to parents that good plaque control is the key for this treatment The recall interval for these patients is every 3 months.
Intervention Type
Procedure
Intervention Name(s)
Conventional Restoration
Intervention Description
Technique: Local anesthesia should be used when needed Perform complete caries removal and cavity preparation Use a matrix band and a wedge to tightly hold the band against the tooth Place the material (Compomer) Check contacts and occlusion, and polish the restoration
Primary Outcome Measure Information:
Title
Failure Rate of the Three Treatment Arms Judged Clinically
Description
Failure rate of the three treatment arms judged clinically after 2 years such as clear caries progression, secondary caries, loss of restoration, reversible pulpitis treated without requiring pulpotomy
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Number of Children Experiencing Irreversible Pulpitis, Dental Abscess, or Extraction
Description
Number of children experiencing irreversible pulpitis, dental abscess, or extraction judged clinically after 2 years
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
Oral Health Status
Description
Child's oral health status as assessed by the gingival status and bacterial plaque index judged clinically after 1 and 2 years
Time Frame
1 and 2 years
Title
Number of Participants With Negative and Positive Behavior During Treatment
Description
Behaviour of children during treatment was assessed using the Frankl Behavior Rating Scale. It is a four-point scale (definitely negative, negative, positive, definitely positive. This scale ranges from definitely negative behaviour, when the child refuses the treatment (worse outcome) to definitely positive behaviour (best outcome), when the participant is completely cooperative. In this scale a score is not reported, thus categories are not converted into numerical data.
Time Frame
Baseline assessment
Title
Number of Participants Reporting Pain Experience During Treatment
Description
Child's perception of pain intensity during treatment was assessed using the Visual Analogue Scale of Faces. It is a five-point scale (1 to 5), which includes five faces of children representing from very light to very intense pain (very low, low, moderate, intense, very intense), with higher scores representing worst outcomes (pain) and low scores best outcomes (no pain). Participants were asked to select the face that represents how he/she felt during the procedure.
Time Frame
Baseline assessment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: - Children aged 3-8 years who attend the Preventive and Paediatric Department of Greifswald University, Germany. (Lithuania: children who attend the paediatric dentistry department, Dental Faculty, Lithuanian University of Health Sciences) At least one primary molar tooth with caries into dentine involving two dental surfaces (diagnosed according to the International Caries Detection and Assessment System [ICDAS], codes 3 to 5) Willing to be examined Exclusion Criteria: Clinical or radiographic signs of pulpal or peri-radicular pathology Patients with a systemic disease requiring special considerations during their dental treatment. Parents/children who refuse to participate in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian H Splieth, Prof. Dr.
Organizational Affiliation
University Medicine Greifswald
Official's Role
Study Chair
Facility Information:
Facility Name
Ernst-Moritz-Arndt-Universität Greifswald. Dental Faculty, Preventive and Paediatric Dentistry Department
City
Greifswald
State/Province
Mecklenburg-Vorpommern
ZIP/Postal Code
17487
Country
Germany
Facility Name
Lithuanian University of Health Sciences, Dental Faculty, Clinic of Dental and Oral Pathology
City
Kaunas
Country
Lithuania
Facility Name
University of Dundee, Dentistry & Nursing , College of Medicine, Unit of Dental and Oral Health School of Dentistry
City
Dundee
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25216660
Citation
Santamaria RM, Innes NP, Machiulskiene V, Evans DJ, Splieth CH. Caries management strategies for primary molars: 1-yr randomized control trial results. J Dent Res. 2014 Nov;93(11):1062-9. doi: 10.1177/0022034514550717. Epub 2014 Sep 12.
Results Reference
result
PubMed Identifier
24602167
Citation
Santamaria RM, Innes NP, Machiulskiene V, Evans DJ, Alkilzy M, Splieth CH. Acceptability of different caries management methods for primary molars in a RCT. Int J Paediatr Dent. 2015 Jan;25(1):9-17. doi: 10.1111/ipd.12097. Epub 2014 Mar 7.
Results Reference
result
PubMed Identifier
29258064
Citation
Santamaria RM, Innes NPT, Machiulskiene V, Schmoeckel J, Alkilzy M, Splieth CH. Alternative Caries Management Options for Primary Molars: 2.5-Year Outcomes of a Randomised Clinical Trial. Caries Res. 2017;51(6):605-614. doi: 10.1159/000477855. Epub 2017 Dec 20.
Results Reference
derived

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European Study on Three Different Approaches to Managing Class 2 Cavities in Primary Teeth

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