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Pulpotomy vs.Root Canal Treatment in Managing Irreversible Pulpitis

Primary Purpose

Pulpitis - Irreversible

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
pulpotomy
Root canal treatment
Sponsored by
King's College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulpitis - Irreversible

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • • Dental patients from an acute (secondary care) setting from at least three UK centres (including King's College London Dental Institute, Denmark Hill and Liverpool).

    • Male or female (aged >16) able to provide informed consent in otherwise good general health with at least one molar tooth with clinical symptoms of irreversible pulpitis caused by caries, requiring RoCT (endodontic treatment).
    • Patients enrolled will have clinical symptoms of irreversible pulpitis who need treatment.

Exclusion Criteria: Exclusion Criteria:

  • The presence of fistulas or swelling
  • Anterior teeth or premolars
  • External or internal root resorption
  • Multiple teeth with carious lesions in the same quadrant,
  • Pregnant women, in view of requirements for radiographs.
  • Patients younger than 16.
  • Patients unable to give consent.
  • Patients who have been administered antibiotics in the previous month.
  • Immunocompromised patients
  • Teeth with hopeless prognosis with caries extended into root dentine and with tooth margin at crestal bone level

Sites / Locations

  • Royal Liverpool University Hospital
  • Guy's HospitalRecruiting
  • King's College HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

experimental pulpotomy

Root canal treatment

Arm Description

Outcomes

Primary Outcome Measures

Short term pain following pulpotomy versus root canal treatment
Pain, tenderness or swelling assessment at baseline and over the first 7 days post completion of treatment using a daily diary of pain (based on a 10 point visual analogue (VAS Scale), measured using the area under the curve (AUC) approach).

Secondary Outcome Measures

Cost-effectiveness of pulpotomy
• Health care resource use between randomization and 12 months post randomization for assessing the cost-effectiveness of pulpotomy in comparison to RCT as measured by the incremental cost-effectiveness ratio (ICER) in terms of the INMB
sensitivity and specificity of CBCT versus periodical radiographs to detect periapical radiolucencies
the sensitivity and specificity of periapical radiograph (clinical standard) to CBCT (experimental) in terms of detection of periapical disease.
success rates of pulpotomy compared to root canal treatment
The vitality or absence of apical pathology of the tooth at 24 months: that is, an absence of either pain, swelling or tenderness to biting of the tooth and no evi-dence of inflammation in the tissues around the tip of the root detected by con-ventional radiographs and CBCT (independent assessors) after 24 months from randomisation. Both assessors must agree to conclude an overall absence of apical pathology. Treatment outcome will be assessed objectively using scans taken pre-treatment and and follow-up (6,12,24 months) appointments.
Quality of life difference between patients that receive pulpotomy versus root canal treatment
• The EQ-5D-3L and EQ-5D-5L measured at baseline, over the first 7 days, 6 and 12 months post randomisation. One major feature of the EQ-5D tool is that the health states obtained from the questionnaire may be con-verted into a single index value with country specific value sets. This will facilitate the calculation and comparison of quality-adjusted life years (QALYs) between pulpotomy vs. primary root canal treatment. The QALY is a measure of disease burden including the quality and quantity of life lived, with one QALY equating to one year in perfect health

Full Information

First Posted
May 14, 2019
Last Updated
November 9, 2020
Sponsor
King's College London
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1. Study Identification

Unique Protocol Identification Number
NCT03956199
Brief Title
Pulpotomy vs.Root Canal Treatment in Managing Irreversible Pulpitis
Official Title
Managing Irreversible Pulpitis - The Effectiveness of Pulpotomy Compared to Root Canal Treatment as a Replacement for Conventional Root Canal Treatment: A Multicentre Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
April 1, 2023 (Anticipated)
Study Completion Date
April 1, 2023 (Anticipated)

3. Sponsor/Collaborators

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

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 study aims to compare two methods of repairing and saving a badly damaged or infected tooth. One method is called root canal treatment (RoCT) and the other (new method) is called pulpotomy. RoCT involves removing the damaged area of the tooth including the tooth nerve (called the pulp), cleaning, disinfecting and sealing it. Pulpotomy however attempts to preserve as much of the tooth nerve as possible (keeping the tooth alive). RoCT is more expensive and painful. Therefore, some patients delay or avoid getting treated, resulting in later complications treated in an emergency setting. This research will aim to show that pulpotomy is less painful, less involved (i.e. less invasive), less time consuming and consequently more cost effective. Long term costs of dental treatment as well as the improved quality of life will therefore offer benefits for patients, public and the NHS who use dental services. Caries (tooth decay) is the most common diseases in the world. The NHS spends at least £3.4 billion per year on dental visits or at dental hospitals. This does not include private (societal) costs to individuals who do not qualify for NHS dental treatment. Consequently, those who end up avoiding or delaying treatment result in complications often treated through the NHS. We have therefore chosen a randomized controlled trial design, a gold standard method to compare the effectiveness of the two treatment options. The participants will be 168 dental patients (male or female) from different parts (London and Liverpool) of the UK so that results can be generalized. This design was considered in consultation with a member of the public (a co-applicant) who will be involved in the trial from the start to completion. The results will be published and discussed at conferences as well as through our patient and public network.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulpitis - Irreversible

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
experimental pulpotomy
Arm Type
Experimental
Arm Title
Root canal treatment
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
pulpotomy
Intervention Description
removal of the pulp from pulp chamber
Intervention Type
Procedure
Intervention Name(s)
Root canal treatment
Intervention Description
Removal of at the entire content of the root canal system and root canal obturation
Primary Outcome Measure Information:
Title
Short term pain following pulpotomy versus root canal treatment
Description
Pain, tenderness or swelling assessment at baseline and over the first 7 days post completion of treatment using a daily diary of pain (based on a 10 point visual analogue (VAS Scale), measured using the area under the curve (AUC) approach).
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Cost-effectiveness of pulpotomy
Description
• Health care resource use between randomization and 12 months post randomization for assessing the cost-effectiveness of pulpotomy in comparison to RCT as measured by the incremental cost-effectiveness ratio (ICER) in terms of the INMB
Time Frame
2 years
Title
sensitivity and specificity of CBCT versus periodical radiographs to detect periapical radiolucencies
Description
the sensitivity and specificity of periapical radiograph (clinical standard) to CBCT (experimental) in terms of detection of periapical disease.
Time Frame
2 years
Title
success rates of pulpotomy compared to root canal treatment
Description
The vitality or absence of apical pathology of the tooth at 24 months: that is, an absence of either pain, swelling or tenderness to biting of the tooth and no evi-dence of inflammation in the tissues around the tip of the root detected by con-ventional radiographs and CBCT (independent assessors) after 24 months from randomisation. Both assessors must agree to conclude an overall absence of apical pathology. Treatment outcome will be assessed objectively using scans taken pre-treatment and and follow-up (6,12,24 months) appointments.
Time Frame
2 years
Title
Quality of life difference between patients that receive pulpotomy versus root canal treatment
Description
• The EQ-5D-3L and EQ-5D-5L measured at baseline, over the first 7 days, 6 and 12 months post randomisation. One major feature of the EQ-5D tool is that the health states obtained from the questionnaire may be con-verted into a single index value with country specific value sets. This will facilitate the calculation and comparison of quality-adjusted life years (QALYs) between pulpotomy vs. primary root canal treatment. The QALY is a measure of disease burden including the quality and quantity of life lived, with one QALY equating to one year in perfect health
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: • Dental patients from an acute (secondary care) setting from at least three UK centres (including King's College London Dental Institute, Denmark Hill and Liverpool). Male or female (aged >16) able to provide informed consent in otherwise good general health with at least one molar tooth with clinical symptoms of irreversible pulpitis caused by caries, requiring RoCT (endodontic treatment). Patients enrolled will have clinical symptoms of irreversible pulpitis who need treatment. Exclusion Criteria: Exclusion Criteria: The presence of fistulas or swelling Anterior teeth or premolars External or internal root resorption Multiple teeth with carious lesions in the same quadrant, Pregnant women, in view of requirements for radiographs. Patients younger than 16. Patients unable to give consent. Patients who have been administered antibiotics in the previous month. Immunocompromised patients Teeth with hopeless prognosis with caries extended into root dentine and with tooth margin at crestal bone level
Facility Information:
Facility Name
Royal Liverpool University Hospital
City
Liverpool
ZIP/Postal Code
L78XP
Country
United Kingdom
Individual Site Status
Active, not recruiting
Facility Name
Guy's Hospital
City
London
ZIP/Postal Code
SE19RT
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francesco Mannocci, Prof
Phone
02011881573
Email
francesco.mannocci@kcl.ac.uk
First Name & Middle Initial & Last Name & Degree
Tiago Pimentel
Facility Name
King's College Hospital
City
London
ZIP/Postal Code
SE5 9RS
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francesco Mannocci
Phone
02011881573
Email
francesco.mannocci@kcl.ac.uk
First Name & Middle Initial & Last Name & Degree
Tiago Pimentel

12. IPD Sharing Statement

Plan to Share IPD
No

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Pulpotomy vs.Root Canal Treatment in Managing Irreversible Pulpitis

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