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The Effect of Different Lining Strategies on Amalgam Restorations

Primary Purpose

Post-operative Pain, Dental Caries

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
No lining
Calcium Hydroxide cement
RMGI cement
Resin Bonding Agent
Sponsored by
University of Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-operative Pain

Eligibility Criteria

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

Inclusion Criteria:

  • Healthy adults over 18 years
  • Presence of one or more carious cavities extending beyond the outer 1/3 of the dentine
  • Able to give valid consent to participate in study
  • Willing to receive an amalgam restoration in a target tooth
  • Teeth free from pain
  • Teeth with vital pulps

Exclusion Criteria:

  • Replacement restorations
  • Psychiatric conditions or medication which may affect pain perception.
  • Cavities limited to the outer ⅓ of dentine.
  • Teeth with existing symptoms or sensitivity
  • Patients under 18 years
  • Non-vital teeth
  • Allergy or idiosyncratic reaction to the study materials
  • Inability to return for review
  • Fractured or cracked teeth
  • Pregnancy or breast-feeding

Sites / Locations

  • University of Birmingham, School of DentistryRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

No lining

Calcium hydroxide cement

Bonding agent

RMGI cement

Arm Description

No lining material placed under amalgam dental restoration

Placement of calcium hydroxide cement under amalgam dental restorations

Placement of Resin bonding agent under amalgam dental restorations

Placement of rmgi lining under amalgam dental restorations

Outcomes

Primary Outcome Measures

Post-operative sensitivity
pain following placement reported by patient using a visual analog scale

Secondary Outcome Measures

Condition of test teeth
Pulp vitality assessed using an electronic pulp tester
Condition of restorations
condition of restorations assessed visually using United States Public Health Service criteria

Full Information

First Posted
April 21, 2015
Last Updated
May 5, 2015
Sponsor
University of Birmingham
Collaborators
Shirley Glasstone Hughes Trust Fund
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1. Study Identification

Unique Protocol Identification Number
NCT02435459
Brief Title
The Effect of Different Lining Strategies on Amalgam Restorations
Official Title
The Effect of Different Lining Strategies on Amalgam Restorations
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Unknown status
Study Start Date
April 2012 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Birmingham
Collaborators
Shirley Glasstone Hughes Trust Fund

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this research is to compare the clinical outcome of amalgam restorations placed in conjunction with three different lining protocols, each of which represents a different therapeutic concept.
Detailed Description
Patients attending one of eight, United Kingdom general dental practitioners for a new restoration in a posterior tooth will be recruited and informed consent obtained. Each dentist will place 20 amalgam restorations either unlined (control), or lined with calcium hydroxide cement, rmgi cement, or sealed with a resin bonding agent (total - 640). Pre-operative radiographs and pulp testing will be performed and measurement of cavity size to assess the remaining dental thickness. The pulp status and symptoms will be recorded at 6, 12, and 24 months. Post-operative sensitivity will be recorded by the patient at 1, 3, 7, 14 and 28 days using a visual analogue scale and diary. The dentists will be trained and calibrated to use United States Public Health Service criteria and the condition of the restoration will be assessed at 12 and 24 months. For each lining option, one product and one admixed amalgam will be provided for use by all the dentists. Training and instruction will be given on the application of the liners and on amalgam condensation to increase standardisation. The collected data will be assessed to identify any association between the outcome variables and the pre-treatment tooth condition or lining material used using logistic regression (α=0.05).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-operative Pain, Dental Caries

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
No lining
Arm Type
Placebo Comparator
Arm Description
No lining material placed under amalgam dental restoration
Arm Title
Calcium hydroxide cement
Arm Type
Active Comparator
Arm Description
Placement of calcium hydroxide cement under amalgam dental restorations
Arm Title
Bonding agent
Arm Type
Active Comparator
Arm Description
Placement of Resin bonding agent under amalgam dental restorations
Arm Title
RMGI cement
Arm Type
Active Comparator
Arm Description
Placement of rmgi lining under amalgam dental restorations
Intervention Type
Procedure
Intervention Name(s)
No lining
Intervention Description
No lining material placed under amalgam dental restorations
Intervention Type
Procedure
Intervention Name(s)
Calcium Hydroxide cement
Intervention Description
placement of lining material under amalgam dental restorations
Intervention Type
Procedure
Intervention Name(s)
RMGI cement
Intervention Description
placement of lining material under amalgam dental restorations
Intervention Type
Procedure
Intervention Name(s)
Resin Bonding Agent
Intervention Description
placement of lining material under amalgam dental restorations
Primary Outcome Measure Information:
Title
Post-operative sensitivity
Description
pain following placement reported by patient using a visual analog scale
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Condition of test teeth
Description
Pulp vitality assessed using an electronic pulp tester
Time Frame
24 months
Title
Condition of restorations
Description
condition of restorations assessed visually using United States Public Health Service criteria
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy adults over 18 years Presence of one or more carious cavities extending beyond the outer 1/3 of the dentine Able to give valid consent to participate in study Willing to receive an amalgam restoration in a target tooth Teeth free from pain Teeth with vital pulps Exclusion Criteria: Replacement restorations Psychiatric conditions or medication which may affect pain perception. Cavities limited to the outer ⅓ of dentine. Teeth with existing symptoms or sensitivity Patients under 18 years Non-vital teeth Allergy or idiosyncratic reaction to the study materials Inability to return for review Fractured or cracked teeth Pregnancy or breast-feeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dominic A Stewardson, PhD
Phone
0121 4665489
Email
d.a.stewardson@bham.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Kirsty B Hill, PhD
Phone
0121 4665488
Email
K.B.Hill@bham.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dominic A Stewardson, PhD
Organizational Affiliation
University of Birmingham, School of Dentistry
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Birmingham, School of Dentistry
City
Birmingham
State/Province
West Midlands
ZIP/Postal Code
B4 6NN
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dominic A Stewardson, PhD
Phone
0121 4665489
Email
d.a.stewardson@bham.ac.uk
First Name & Middle Initial & Last Name & Degree
Kirsty B Hill, PhD
Phone
0121 4665488
Email
K.B.Hill@bham.ac.uk

12. IPD Sharing Statement

Learn more about this trial

The Effect of Different Lining Strategies on Amalgam Restorations

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