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Selective or Stepwise Removal of Deep Caries

Primary Purpose

Dental Caries

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Selective removal
Stepwise removal
Sponsored by
Charite University, Berlin, Germany
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dental Caries

Eligibility Criteria

3 Years - 9 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children 3-9 yr
  • Good general health
  • Minimum one active deep (D3) occlusal/occlusal-proximal, one-/two-surface caries lesion

Exclusion Criteria:

  • Participating in other study
  • Plan to move or not resident
  • Systemic disease or general disability
  • Expected limited compliance
  • Known allergy to study material expected exfoliation within 18 month

Sites / Locations

  • Ernst-Moritz-Arndt University of Greifswald, Präventive Zahnmedizin und Kinderzahnheilkunde
  • Uniklinik RWTH Aachen; Klinik für Zahnerhaltung, Parodontologie und Präventive ZahnheilkundeRecruiting
  • CharitéCentrum für Zahn-, Mund- und Kieferheilkunde der Charité - Universitätsmedizin Berlin, Abteilung für Kieferorthopädie, Orthodontie und KinderzahnmedizinRecruiting
  • CharitéCentrum für Zahn-, Mund- und Kieferheilkunde der Charité - Universitätsmedizin Berlin; Abteilungen für Zahnerhaltung und Präventive ZahnheilkundeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Selective removal

Stepwise removal

Arm Description

Outcomes

Primary Outcome Measures

Success (re-intervention required no/yes)
The primary outcome of the study will be success (i. e. not requiring any re-intervention).

Secondary Outcome Measures

Survival (tooth removal required no/yes)
Secondary outcomes will include survival (i. e. not requiring extraction).
Restoration integrity (scored as alpha, beta, gamma, delta)
Restoration integrity will be assessed via modified USPHS-criteria.
Patients' subjective assessment of the treatment (0-10)
Patients' subjective assessment of the treatment will be recorded using visual-analogue scale. For stepwise excavation, assessments will be performed twice and mean VAS-results calculated.
Dentists' subjective assessment (1-6)
Dentists' subjective assessment of the treatment will be reported using grades from 1 (very good) to 6 (very bad).
Parents' subjective assessment (1-6)
similar to dentists' assessment
Treatment costs (Euro)
Total treatment costs (calculated by combining costs for staff, as assessed by time required for the procedures and the number of personnel involved, and costs for transportation of patients or materials) for both initial and follow-up treatments.

Full Information

First Posted
August 29, 2014
Last Updated
July 27, 2015
Sponsor
Charite University, Berlin, Germany
Collaborators
Rheinisch-Westfälische Technische Hochschule RWTH Aachen, Germany, University Medicine Greifswald
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1. Study Identification

Unique Protocol Identification Number
NCT02232828
Brief Title
Selective or Stepwise Removal of Deep Caries
Official Title
Selective or Stepwise Removal of Deep Caries in Deciduous Molars: A Multi-center Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Unknown status
Study Start Date
October 2014 (undefined)
Primary Completion Date
October 2017 (Anticipated)
Study Completion Date
June 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Charite University, Berlin, Germany
Collaborators
Rheinisch-Westfälische Technische Hochschule RWTH Aachen, Germany, University Medicine Greifswald

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: For treating deep caries lesions, selective or stepwise, i. e. one- and two-step incomplete excavation seems advantageous compared with complete caries removal. However, current evidence regarding the success, as defined by not requiring any re-treatments, or survival of teeth after different excavations is insufficient for definitive recommendation, especially when treating deciduous teeth. Moreover, restoration integrity has not been comparatively analyzed longitudinally, and neither patients', dentists' or parents' preferences nor the clinical long-term costs emanating from both initial and re-treatments have been reported yet. Our primary hypothesis is that success rates differ significantly between selectively and stepwise excavated teeth. Secondary hypotheses are that restoration integrity is assumed to significantly differ between selectively and stepwise excavated teeth.
Detailed Description
The treatment of deep caries lesions is associated with significant risks for the pulp, including pulpal exposure and post-operative pulpal complications, which might eventually compromise the retention of the tooth [1]. Moreover, treating deep lesions might be associated with pain and subjective burden both during and after treatment and might generate long-term costs due to re-treatments being required [2, 3]. For deciduous teeth, various treatments for deep lesions have been described: Complete excavation aims at removing all infected and affected carious dentin, with the inherent risk of pulpal exposure. In contrast, stepwise, i. e. two-step excavation leaves carious dentin after the initial excavation step, then seals residual caries under a temporary restoration, and re-enters the cavity in a second step to eventually attempt complete excavation. This approach is thought to facilitate arrest and remineralization of the lesion and to induce development of tertiary dentin, thereby reducing the risk of pulpal exposure and post-operative complications after the second excavation step [4, 5]. Since several studies found sealed residual lesions to be clinically and microbiologically arrested, the need to re-enter was increasingly questioned within the last decade [6]. Selective, i. e. one-step incomplete or partial excavation seals carious dentin under a definitive restoration, omitting any re-entry [7]. Sealing the lesion is thought to deprive residual bacteria from dietary carbohydrates and was found to exert significant antibacterial effects, thus arresting the lesion [8, 9]. However, doubts remain regarding the effects of sealed carious dentin on the long-term quality of the restoration [10]. Moreover, it remains unknown if patients prefer one of both treatments, which might be especially relevant when treating children. Several studies comparing complete with selective or stepwise excavation of deciduous teeth have been published, but only one three-arm study compared selective with stepwise excavation of primary teeth (Tab. 1). In addition, none of these studies assessed patient- or dentists-centered outcomes, i. e. preferences, or analyzed clinically assessed long-term costs emanating from both excavations. Objectives and Hypotheses The study aims at comparing the success, i. e. the probability of not requiring any re-interventions, and the survival, i. e. the probability of not requiring tooth removal, of selectively versus stepwise excavated vital, non-symptomatic deciduous molars with deep lesions. In addition, we assess the restoration integrity of selectively versus stepwise excavated deciduous molars, evaluate the preference of patients, parents and dentists for one of both strategies, and comparatively assess the costs associated with each strategy. Our primary hypothesis is that success rates differ significantly between selectively and stepwise excavated teeth. Secondary hypotheses are that restoration integrity is assumed to significantly differ between selectively and stepwise excavated teeth. Moreover, we hypothesize that patients', parents' and dentists' preference is significantly different for selective versus stepwise excavated teeth. Eventually, both initial and long-term costs of excavation methods are supposed to significantly differ. The planned study is a secondary care-based prospective, multi-center two-arm, parallel-group, randomized controlled trial at three pediatric university dental clinics in Germany. We plan to enroll 300 patients with one or more deeply carious, sensitive and non-symptomatic deciduous molar. One molar per patient will be randomly allocated to receive one of two treatments (selective or stepwise excavation). Total follow-up time will be three years after completion of the initial treatment. Success, survival and restoration integrity will be assessed after one, two and three years. Patients', parents' and dentists' preference will be assessed after each treatment using visual-analogue scale or Likert-rating scales. Costs will be assessed for initial and follow-up treatments and will be based on a micro-costing approach.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Selective removal
Arm Type
Experimental
Arm Title
Stepwise removal
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Selective removal
Intervention Description
Caries removal in the periphery including the enamel-dentinal junction will be performed using rose head burs and/or an excavator until hard, dry dentin remains. Pulpo-proximal caries will be removed until leathery, slightly moist and reasonably soft dentin remains. Operating dentists will be calibrated prior to study commencement regarding these criteria using extracted teeth. Moisture control will be performed using cotton rolls and continuous aspiration. Restoration will be performed adhesively, with a self-etching one-bottle adhesive (G-aenial bond, GC, Bad Homburg, Germany) and a compomer material (Dyract, Dentsply Detray, Konstanz, Germany) being used.
Intervention Type
Procedure
Intervention Name(s)
Stepwise removal
Intervention Description
Caries removal in the periphery including the enamel-dentinal junction will be performed using rose head burs and/or an excavator until hard, dry dentin remains. Pulpo-proximal caries will be removed until leathery, slightly moist and reasonably soft dentin remains. Operating dentists will be calibrated prior to study commencement regarding these criteria using extracted teeth. Moisture control will be performed using cotton rolls and continuous aspiration. Restoration will be performed adhesively, with a self-etching one-bottle adhesive (G-aenial bond, GC, Bad Homburg, Germany) and a compomer material (Dyract, Dentsply Detray, Konstanz, Germany) being used. If allocated to stepwise excavation, the second excavation will now be performed as described until only hard, dry dentin remains. Restoration will again be provided adhesively as described.
Primary Outcome Measure Information:
Title
Success (re-intervention required no/yes)
Description
The primary outcome of the study will be success (i. e. not requiring any re-intervention).
Time Frame
36 month
Secondary Outcome Measure Information:
Title
Survival (tooth removal required no/yes)
Description
Secondary outcomes will include survival (i. e. not requiring extraction).
Time Frame
36 months
Title
Restoration integrity (scored as alpha, beta, gamma, delta)
Description
Restoration integrity will be assessed via modified USPHS-criteria.
Time Frame
36 months
Title
Patients' subjective assessment of the treatment (0-10)
Description
Patients' subjective assessment of the treatment will be recorded using visual-analogue scale. For stepwise excavation, assessments will be performed twice and mean VAS-results calculated.
Time Frame
0 months (directly after treatment)
Title
Dentists' subjective assessment (1-6)
Description
Dentists' subjective assessment of the treatment will be reported using grades from 1 (very good) to 6 (very bad).
Time Frame
0 months (directly after treatment)
Title
Parents' subjective assessment (1-6)
Description
similar to dentists' assessment
Time Frame
0 months (directly after treatment)
Title
Treatment costs (Euro)
Description
Total treatment costs (calculated by combining costs for staff, as assessed by time required for the procedures and the number of personnel involved, and costs for transportation of patients or materials) for both initial and follow-up treatments.
Time Frame
36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children 3-9 yr Good general health Minimum one active deep (D3) occlusal/occlusal-proximal, one-/two-surface caries lesion Exclusion Criteria: Participating in other study Plan to move or not resident Systemic disease or general disability Expected limited compliance Known allergy to study material expected exfoliation within 18 month
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Falk Schwendicke, OA Dr.
Phone
+4930450562
Ext
556
Email
falk.schwendicke@charite.de
First Name & Middle Initial & Last Name or Official Title & Degree
Sebastian Paris, Prof. Dr.
Phone
+4930450562
Ext
332
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Falk Schwendicke, OA Dr.
Organizational Affiliation
Chatrite Berlin, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sebastian Paris, Prof. Dr.
Organizational Affiliation
Charite Berlin, Germany
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Christian Finke, OA Dr.
Organizational Affiliation
Charite Berlin, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marina A. Petrou, Dr.
Organizational Affiliation
Uniklinic RWTH Aachen, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christian Spleith, Prof. Dr.
Organizational Affiliation
University Greifswald, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ruth Santamaria, Dr.
Organizational Affiliation
University Greifswald, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ernst-Moritz-Arndt University of Greifswald, Präventive Zahnmedizin und Kinderzahnheilkunde
City
Greifswald
State/Province
Mecklenburg Vorpommern
ZIP/Postal Code
17487
Country
Germany
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christian Splieth, Prof. Dr.
First Name & Middle Initial & Last Name & Degree
Ruth Santamaria, Dr.
First Name & Middle Initial & Last Name & Degree
Christian Splieth, Prof. Dr.
First Name & Middle Initial & Last Name & Degree
Ruth Santamaria, Dr.
Facility Name
Uniklinik RWTH Aachen; Klinik für Zahnerhaltung, Parodontologie und Präventive Zahnheilkunde
City
Aachen
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
52074
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marina A. Petrou, Dr.
First Name & Middle Initial & Last Name & Degree
Marina A. Petrou, Dr.
Facility Name
CharitéCentrum für Zahn-, Mund- und Kieferheilkunde der Charité - Universitätsmedizin Berlin, Abteilung für Kieferorthopädie, Orthodontie und Kinderzahnmedizin
City
Berlin
ZIP/Postal Code
14197
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christian Finke, OA Dr.
Phone
+49450562
Ext
0
Email
Christian.Finke@charite.de
First Name & Middle Initial & Last Name & Degree
Christian Finke, OA Dr.
Facility Name
CharitéCentrum für Zahn-, Mund- und Kieferheilkunde der Charité - Universitätsmedizin Berlin; Abteilungen für Zahnerhaltung und Präventive Zahnheilkunde
City
Berlin
ZIP/Postal Code
14197
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Falk Schwendicke, OA Dr.
Phone
+4930450562
Ext
556
Email
falk.schwenicke@charite.de
First Name & Middle Initial & Last Name & Degree
Sebastian Paris, Prof. Dr.
Phone
+4930450562
Ext
332
Email
sebastian.paris@charite.de
First Name & Middle Initial & Last Name & Degree
Falk Schwendicke, OA Dr.

12. IPD Sharing Statement

Citations:
PubMed Identifier
32857210
Citation
Elhennawy K, Finke C, Paris S, Reda S, Jost-Brinkmann PG, Schwendicke F. Selective vs stepwise removal of deep carious lesions in primary molars: 24 months follow-up from a randomized controlled trial. Clin Oral Investig. 2021 Feb;25(2):645-652. doi: 10.1007/s00784-020-03536-6. Epub 2020 Aug 28.
Results Reference
derived
PubMed Identifier
30025748
Citation
Elhennawy K, Finke C, Paris S, Reda S, Jost-Brinkmann PG, Schwendicke F. Selective vs stepwise removal of deep carious lesions in primary molars: 12-Months results of a randomized controlled pilot trial. J Dent. 2018 Oct;77:72-77. doi: 10.1016/j.jdent.2018.07.011. Epub 2018 Jul 17.
Results Reference
derived
PubMed Identifier
25560779
Citation
Schwendicke F, Schweigel H, Petrou MA, Santamaria R, Hopfenmuller W, Finke C, Paris S. Selective or stepwise removal of deep caries in deciduous molars: study protocol for a randomized controlled trial. Trials. 2015 Jan 6;16:11. doi: 10.1186/s13063-014-0525-9.
Results Reference
derived

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Selective or Stepwise Removal of Deep Caries

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