search
Back to results

Root Caries Excavation With Air Water/Powder Prophylaxis Device for ART Restorations (ART-AIRFLOW)

Primary Purpose

Dental Caries Extending Into Dentin, Root Caries

Status
Not yet recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Control: Hand instrumentation for caries excavation
Intervention 1: EMS Airflow device for caries excavation
Intervention 2: Hand excavation + EMS Airflow device for caries excavation
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dental Caries Extending Into Dentin focused on measuring Root caries, Elders, Atraumatic restorative treatment, Glass-ionomer cement

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria

  • Adults ≥65 years
  • Dentinal root caries lesions with no painful symptomology
  • Can follow instructions for oral hygiene
  • Not dependent for care for their ADLs.

Exclusion criteria:

  • Symptomatic carious teeth
  • Non-carious attrition, erosion or abrasion cavities
  • Periodontally compromised teeth with Grade 3 mobility, and active signs of infections.
  • Not willing or able to sign informed consent

Post-hoc exclusion:

  • Participant withdraws consent
  • Medical reasons.

Sites / Locations

  • Clinic of General, Special care, and Geriatric Dentistry, Center of Dental Medicine, University of Zurich

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Experimental

Experimental

Arm Label

Control: Hand instrumentation for caries excavation

Intervention 1: EMS Airflow device for caries excavation

Intervention 2: Hand excavation + EMS Airflow device for caries excavation

Arm Description

Hand instrumentation for caries excavation

Powder/water jet prophylaxis device (EMS Airflow) for caries excavation

Hand excavation and Powder/ jet prophylaxis device (EMS Airflow) for caries excavation

Outcomes

Primary Outcome Measures

Restoration Success rate
Restoration success rate (SxR %): For the purpose of this trial, a successful restoration is defined as one that has undergone no changes in its surface / structural integrity, still adhered to the structure and is functional when examined during the scheduled or unscheduled recall visit. The restoration success rate (SxR %) is calculated by the number of successful restorations present at the end of the trial (nsx) divided by the number of restorations placed in the beginning of the trial (N0) multiplied by 100 using the formula: SxR % = (nsx / N0) * 100.
Restoration survival rate
Restoration survival rate (SvR %): For the purpose of this trial, any restoration, where the surface or structural integrity is compromised, but still adhering to the tooth, is functional and does not warrant a repair or replacement when examined during the scheduled or unscheduled recall visit, is considered survived. The restoration survival rate (SvR %) is calculated by the number of survived restorations present at the end of the trial (nsv) divided by the number of restorations placed in the beginning of the trial (N0) multiplied by 100 using the formula: SvR = (nsv / N0) * 100.

Secondary Outcome Measures

Participants' Treatment preference
Secondary assessment will be to assess the participants' treatment preference. This is done by administering a simple questionnaire which inquires on their treatment preferences. After treatment will be completed the dental nurse will question the participant about their treatment preference. The questions will include preferences for restorative treatment with or without the use of anaesthesia, with or without rotary instrumentation, hand instrumentation or with air-water prophylaxis device, compared to their previous dental experience. The response "no difference" will also an option.

Full Information

First Posted
March 16, 2021
Last Updated
March 25, 2021
Sponsor
University of Zurich
search

1. Study Identification

Unique Protocol Identification Number
NCT04822246
Brief Title
Root Caries Excavation With Air Water/Powder Prophylaxis Device for ART Restorations
Acronym
ART-AIRFLOW
Official Title
Excavation of Root Caries With Air-water Powder Stream vs Manual Excavation for Atraumatic Restorative Treatment in Older Patients: a Single-blind Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2021 (Anticipated)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of this RCT is to compare the efficacy of a powder/water jet prophylaxis device and conventional hand excavation in excavating root surface caries, with regard to restoration survival/success in older adults. The secondary outcome of this RCT is to assess the participants' treatment preferences for the received treatment with regard to the procedures involved and in the invasiveness of the procedures carried out during the ART restoration.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries Extending Into Dentin, Root Caries
Keywords
Root caries, Elders, Atraumatic restorative treatment, Glass-ionomer cement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Single-blind, RCT
Masking
Participant
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control: Hand instrumentation for caries excavation
Arm Type
Other
Arm Description
Hand instrumentation for caries excavation
Arm Title
Intervention 1: EMS Airflow device for caries excavation
Arm Type
Experimental
Arm Description
Powder/water jet prophylaxis device (EMS Airflow) for caries excavation
Arm Title
Intervention 2: Hand excavation + EMS Airflow device for caries excavation
Arm Type
Experimental
Arm Description
Hand excavation and Powder/ jet prophylaxis device (EMS Airflow) for caries excavation
Intervention Type
Procedure
Intervention Name(s)
Control: Hand instrumentation for caries excavation
Other Intervention Name(s)
Hand instrumentation for caries excavation
Intervention Description
An enamel hatchet will be used to create access to the carious lesion and then removal of soft carious tissue will be undertaken with excavators. Excavation will be stopped when some resistance to excavation will be felt and the cavity will be then conditioned with polyacrylic acid for 20 s, washed and dried with cotton pellets. A high-viscosity glass-ionomer cement will be used to restore the cavity. Moisture control will be achieved with the use of cotton wool rolls. A chair-side assistant will hand-mix the glass-ionomer according to manufacturers' instructions and it will be placed in the cavity using the "press-finger" technique whenever the type of cavity allows it. In the case of root restorations, a glove coated with petroleum jelly will be used similarly to the "press-finger" technique to better condense the material into the cavity. Excess material will be removed; the restoration will be coated with petroleum jelly. No local anaesthetic will be used to provide ART treatment.
Intervention Type
Procedure
Intervention Name(s)
Intervention 1: EMS Airflow device for caries excavation
Other Intervention Name(s)
Powder/water jet prophylaxis device (EMS Airflow) for caries excavation
Intervention Description
An enamel hatchet will first be used to gain access into the cavity. Then the powder-water prophylaxis device will be used for the removal of soft carious tissue with the sodium bicarbonate powder-water jet. Excavation will be stopped when the colour of the lesion begins to darken and all the soft deposits are evacuated. The excavation will be done intermittently allowing sufficient time to check with hand instrument the surface hardness of the lesion. If the lesion is still soft excavation will be continued until the surface is hard suitable for restoring. The cavity will be then rinsed with copious water spray to evacuate all the powder-water material. The restoration procedure with a glass-ionomer cement will be done following the same procedures as in the control group.
Intervention Type
Procedure
Intervention Name(s)
Intervention 2: Hand excavation + EMS Airflow device for caries excavation
Other Intervention Name(s)
Hand excavation and Powder/ jet prophylaxis device (EMS Airflow) for caries excavation
Intervention Description
The participants allocated to this group will have the caries excavated as described for the control group. Then prior to filling the excavated cavity, the procedure of sodium bicarbonate powder-water jet irrigation as described for the intervention group #1 will be performed to condition the prepared excavated cavity. Then the restorative procedure will be completed with the restorative material and procedures as described for the previous groups.
Primary Outcome Measure Information:
Title
Restoration Success rate
Description
Restoration success rate (SxR %): For the purpose of this trial, a successful restoration is defined as one that has undergone no changes in its surface / structural integrity, still adhered to the structure and is functional when examined during the scheduled or unscheduled recall visit. The restoration success rate (SxR %) is calculated by the number of successful restorations present at the end of the trial (nsx) divided by the number of restorations placed in the beginning of the trial (N0) multiplied by 100 using the formula: SxR % = (nsx / N0) * 100.
Time Frame
1 year, year 1
Title
Restoration survival rate
Description
Restoration survival rate (SvR %): For the purpose of this trial, any restoration, where the surface or structural integrity is compromised, but still adhering to the tooth, is functional and does not warrant a repair or replacement when examined during the scheduled or unscheduled recall visit, is considered survived. The restoration survival rate (SvR %) is calculated by the number of survived restorations present at the end of the trial (nsv) divided by the number of restorations placed in the beginning of the trial (N0) multiplied by 100 using the formula: SvR = (nsv / N0) * 100.
Time Frame
1 year, year 1
Secondary Outcome Measure Information:
Title
Participants' Treatment preference
Description
Secondary assessment will be to assess the participants' treatment preference. This is done by administering a simple questionnaire which inquires on their treatment preferences. After treatment will be completed the dental nurse will question the participant about their treatment preference. The questions will include preferences for restorative treatment with or without the use of anaesthesia, with or without rotary instrumentation, hand instrumentation or with air-water prophylaxis device, compared to their previous dental experience. The response "no difference" will also an option.
Time Frame
Through study completion, an average of 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria Adults ≥65 years Dentinal root caries lesions with no painful symptomology Can follow instructions for oral hygiene Not dependent for care for their ADLs. Exclusion criteria: Symptomatic carious teeth Non-carious attrition, erosion or abrasion cavities Periodontally compromised teeth with Grade 3 mobility, and active signs of infections. Not willing or able to sign informed consent Post-hoc exclusion: Participant withdraws consent Medical reasons.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Murali Srinivasan
Phone
+4144 6343341
Email
murali.srinivasan@zzm.uzh.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Elena van der Heijden
Phone
+41446343341
Email
Elena.vanderHeijden@zzm.uzh.ch
Facility Information:
Facility Name
Clinic of General, Special care, and Geriatric Dentistry, Center of Dental Medicine, University of Zurich
City
Zurich
ZIP/Postal Code
8032
Country
Switzerland

12. IPD Sharing Statement

Learn more about this trial

Root Caries Excavation With Air Water/Powder Prophylaxis Device for ART Restorations

We'll reach out to this number within 24 hrs