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Efficacy of Calcium Silicate Pulp-capping; a Randomized Controlled Clinical Trial

Primary Purpose

Reversible Pulpitis

Status
Unknown status
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Cone Beam computed tomography (Morita Accuitomo)
Periapical radiographs
calcium silicate cement (Biodentine™)
glass ionomer cement ( Fuji IX™)
Sponsored by
King's College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Reversible Pulpitis focused on measuring Indirect pulp capping, reversible pulpitis, periapical radiolucency, periapical radiographs, cone beam computed tomography, calcium silicate cements, glass ionomer cements, caries

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Patients either male or female over the age of 16 (who can consent for themselves) in good general health
  2. A minimum of one carious lesion (occlusal, proximal, or MOD)
  3. Positive pulp response to electric pulp test and thermal stimulation.

Exclusion Criteria:

  1. Patients with clinical symptoms of irreversible pulpitis who need root canal treatment
  2. The presence of fistulas or swelling
  3. Anterior teeth with aesthetic concerns
  4. External or internal root resorption
  5. Multiple teeth with carious lesions in the same quadrant,
  6. Mobile teeth or tenderness to percussion.
  7. Pregnant women, in view of requirements for radiographs.
  8. Patients younger than 16.
  9. Patients unable to give consent

Sites / Locations

  • King's College Dental Institute at Guy's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Active Comparator

Active Comparator

Arm Label

calcium silicate cement (Biodentine™)

Cone Beam computed tomography (CBCT)

Periapical radiographs

Glass ionomer cement ( Fuji IX™)

Arm Description

calcium silicate cement (Biodentine™) used for indirect pulp capping of teeth with deep carious lesions and inflammed pulps.

CBCT scans are taken to assess the efficacy of this method in detecting the presence of early peri-radicular lesions.

Periapical radiographs are taken as a control to detect the presence of early peri-radicular lesions.

Glass ionomer cement ( Fuji IX™) used for indirect pulp capping of teeth with deep carious lesions and inflammed pulps.

Outcomes

Primary Outcome Measures

The principal outcome of the study is whether the tooth restored with the test or control material remains vital (alive) at follow-up examination.
The vitality of the restored tooth (whether the nerve of the tooth is alive or dead) is determined clinically by a positive response to cold test, absence of spontaneous pain, negative sensitivity to percussion, absence of sinus/fistula/swelling and abnormal mobility, and absence/reduction of periapical radiolucencies as determined by PA radiographs.

Secondary Outcome Measures

The integrity of the composite restoration overlying the test or control material is either acceptable or not.
As assessed clinically by USPHS criteria and Hickel's criteria for the assessment of dental restorations.
The CBCT scans of the teeth restored with the test or control material are either more effective or are comparable to conventional radiographs in detecting the presence of early peri-radicular lesions associated with the restored teeth.

Full Information

First Posted
July 23, 2014
Last Updated
March 1, 2017
Sponsor
King's College London
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1. Study Identification

Unique Protocol Identification Number
NCT02201641
Brief Title
Efficacy of Calcium Silicate Pulp-capping; a Randomized Controlled Clinical Trial
Official Title
Efficacy of Calcium Silicate Pulp-capping; a Randomized Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
July 2012 (undefined)
Primary Completion Date
July 2017 (Anticipated)
Study Completion Date
July 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
King's College London

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study aims to investigate the tooth nerve response to a recently introduced therapeutic filling material (calcium silicate cement) called Biodentine and to assess the quality of the overlying filling compared to another material (glass ionomer cement) called Fuji IX used more commonly. Also to compare the effectiveness of cone beam computed tomography x-rays compared to conventional periapical x-rays in detecting lesions around these teeth.
Detailed Description
Tooth decay is one of the most widespread diseases in the world. Very often, a patient comes to the dental clinic when experiencing pain which commonly means the decay is deep and is very close to or has penetrated the nerve of the tooth. When the decay is very close to the pulp or nerve of the tooth, a procedure called pulp capping is done in an attempt to save the tooth and to prevent root canal treatment. A material has been introduced to the market for this purpose, called Biodentine. This study aims to investigate the nerve response to this material and to assess the quality of the overlying filling compared to another material (glass ionomer cement) used more commonly. Also, X-rays are a routine procedure used to assess how close the decay is to the nerve and to see if there are abnormalities around the tooth. However conventional X-rays may not be accurate. A new technique called Cone Beam Computed Tomography (CBCT) has been developed which shows a 3-D image of the tooth and may be more accurate. We aim to compare the images gained from conventional X-rays and CBCT to help improve diagnosis and care planning for patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Reversible Pulpitis
Keywords
Indirect pulp capping, reversible pulpitis, periapical radiolucency, periapical radiographs, cone beam computed tomography, calcium silicate cements, glass ionomer cements, caries

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
calcium silicate cement (Biodentine™)
Arm Type
Experimental
Arm Description
calcium silicate cement (Biodentine™) used for indirect pulp capping of teeth with deep carious lesions and inflammed pulps.
Arm Title
Cone Beam computed tomography (CBCT)
Arm Type
Experimental
Arm Description
CBCT scans are taken to assess the efficacy of this method in detecting the presence of early peri-radicular lesions.
Arm Title
Periapical radiographs
Arm Type
Active Comparator
Arm Description
Periapical radiographs are taken as a control to detect the presence of early peri-radicular lesions.
Arm Title
Glass ionomer cement ( Fuji IX™)
Arm Type
Active Comparator
Arm Description
Glass ionomer cement ( Fuji IX™) used for indirect pulp capping of teeth with deep carious lesions and inflammed pulps.
Intervention Type
Radiation
Intervention Name(s)
Cone Beam computed tomography (Morita Accuitomo)
Intervention Description
CBCT scans are taken to assess the efficacy of this method in detecting the presence of early peri-radicular lesions.
Intervention Type
Radiation
Intervention Name(s)
Periapical radiographs
Intervention Description
Periapical radiographs are taken as a control to detect the presence of early peri-radicular lesions.
Intervention Type
Device
Intervention Name(s)
calcium silicate cement (Biodentine™)
Intervention Description
calcium silicate cement (Biodentine™) used for indirect pulp capping of teeth with deep carious lesions and inflammed pulps.
Intervention Type
Device
Intervention Name(s)
glass ionomer cement ( Fuji IX™)
Intervention Description
glass ionomer cement ( Fuji IX™) used for indirect pulp capping of teeth with deep carious lesions and inflammed pulp.
Primary Outcome Measure Information:
Title
The principal outcome of the study is whether the tooth restored with the test or control material remains vital (alive) at follow-up examination.
Description
The vitality of the restored tooth (whether the nerve of the tooth is alive or dead) is determined clinically by a positive response to cold test, absence of spontaneous pain, negative sensitivity to percussion, absence of sinus/fistula/swelling and abnormal mobility, and absence/reduction of periapical radiolucencies as determined by PA radiographs.
Time Frame
up to 2 years
Secondary Outcome Measure Information:
Title
The integrity of the composite restoration overlying the test or control material is either acceptable or not.
Description
As assessed clinically by USPHS criteria and Hickel's criteria for the assessment of dental restorations.
Time Frame
up to 2 years
Title
The CBCT scans of the teeth restored with the test or control material are either more effective or are comparable to conventional radiographs in detecting the presence of early peri-radicular lesions associated with the restored teeth.
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients either male or female over the age of 16 (who can consent for themselves) in good general health A minimum of one carious lesion (occlusal, proximal, or MOD) Positive pulp response to electric pulp test and thermal stimulation. Exclusion Criteria: Patients with clinical symptoms of irreversible pulpitis who need root canal treatment The presence of fistulas or swelling Anterior teeth with aesthetic concerns External or internal root resorption Multiple teeth with carious lesions in the same quadrant, Mobile teeth or tenderness to percussion. Pregnant women, in view of requirements for radiographs. Patients younger than 16. Patients unable to give consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Timothy F Watson, BDS,MSc,PhD
Organizational Affiliation
King's College London
Official's Role
Study Chair
Facility Information:
Facility Name
King's College Dental Institute at Guy's Hospital
City
London
ZIP/Postal Code
SE1 9RT
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30232625
Citation
Hashem D, Mannocci F, Patel S, Manoharan A, Watson TF, Banerjee A. Evaluation of the efficacy of calcium silicate vs. glass ionomer cement indirect pulp capping and restoration assessment criteria: a randomised controlled clinical trial-2-year results. Clin Oral Investig. 2019 Apr;23(4):1931-1939. doi: 10.1007/s00784-018-2638-0. Epub 2018 Sep 19.
Results Reference
derived
PubMed Identifier
25710953
Citation
Hashem D, Mannocci F, Patel S, Manoharan A, Brown JE, Watson TF, Banerjee A. Clinical and radiographic assessment of the efficacy of calcium silicate indirect pulp capping: a randomized controlled clinical trial. J Dent Res. 2015 Apr;94(4):562-8. doi: 10.1177/0022034515571415. Epub 2015 Feb 20.
Results Reference
derived

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Efficacy of Calcium Silicate Pulp-capping; a Randomized Controlled Clinical Trial

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