search
Back to results

Preformed Pediatric Crown Zirconia Versus Preformed Pediatric Metal Crown (PPC Z-M)

Primary Purpose

Tooth Decay

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
PPC z
PPC m
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tooth Decay

Eligibility Criteria

4 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children of at least 4 years of good general health (ASAI or II),
  • Child with at least two temporary molars of the same type, 1st or 2nd molar, contralateral (fractional mouth), meeting the following criteria:

The two temporary molars are affected by a cavitary carious lesion or a hypoplastic defect of at least 2 faces,

  • the two temporary molars of the pair (54-64, 55-65, 74-84 or 75-85), should or should not be subjected to pulpotomy prior to the realization of the CPP,
  • the two molars must have an antagonistic tooth.

    • Consent of parents (legal guardians) and child,
    • Child and parents (legal guardians) speaking French,
    • Child covered by his parents' social security cover,
    • Child cooperating in the vigilant or sedated state (cooperation evaluated with a Venham score 0, 1, 2).

Exclusion Criteria:

  • Child who does not cooperate in care under vigil or under conscious sedation, who must therefore be treated under general anesthesia.
  • Child allergic to local anesthetics, chromium or nickel. Exclusion dental criteria
  • Primary molar whose physiological exfoliation will appear within 24 months or pimary molar with a root resorption of more than a third of the radicular length.
  • Severely decayed PM prohibiting the retention and the sealing of the restoration.
  • Primary molar with exposed cement or with evidence of swelling in the surrounding tissues
  • Molar with spontaneous pain.
  • Primary molar in infraclusion.
  • Primary molar whose radiographic examination reveals a widening of the desmodontal space, the presence of radiolucent image on the root furcation and/or apices, internal or external resorption

Sites / Locations

  • CHRU LilleRecruiting
  • CHU de NantesRecruiting
  • CHU de NiceRecruiting
  • CHU StransbourgRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

PPC m

PPC z

Arm Description

Outcomes

Primary Outcome Measures

clinical and radiographique observations
Success of the treatment defined by the absence of major failure. A composite measure of signs and symptoms leading to diagnosis of irreversible pulpitis or periradicular periodontitis will be used to define major failure (pain, pulp infection, dental abscess, periradicular pathology visible on radiograph

Secondary Outcome Measures

Full Information

First Posted
July 28, 2017
Last Updated
October 15, 2020
Sponsor
Centre Hospitalier Universitaire de Nice
search

1. Study Identification

Unique Protocol Identification Number
NCT03296709
Brief Title
Preformed Pediatric Crown Zirconia Versus Preformed Pediatric Metal Crown
Acronym
PPC Z-M
Official Title
Preformed Pediatric Crown Zirconia Versus Preformed Pediatric Metal Crown PPC Z-M
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 10, 2018 (Actual)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
March 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

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
Preformed metal pediatric crowns (PPCm) are currently considered the best method of restoring Primary molars affected by severe carious lesions compared to restorations made with various restorative materials (amalgams, composites, CVI-based materials). Due to their unsightly appearance, denounced by many parents, more aesthetic zirconia (PPCz) preformed pediatric crowns have been recently marketed. In the absence of an evaluation of the latter, this multi-center split-mouth two-year randomized clinical trial (RCT) proposes to to investigate the effectiveness of PPCz for the management of dental caries or structural anomalies. More specifically, the primary objective of this RCT is to assess in primary molars the success of PPCz in comparison with PPCm. The control treatment will be PPCm since this is the standard crown option. One hundred children and one aged at least 4 years must be recruited in ninedepartments of Pediatric Dentistry in the university hospitals of Bordeaux, Lille, Nancy, Nantes, Nice, Paris 1&2, Strasbourg and Toulouse. They will be included if they have two similar primarymolars of the same arch (for example first right and left maxillary primary molars ) and equally affected, to be crowned. The two types of crowns to be used in the same child, PPCm(3M Espe) and PPCz(Ezpédo), will be affected by randomization using a computerized and centralized system: primary molars will first be allocated to PPCm and, one to two weeks later, the contralateral primary molar will be restored by PPCz. The children will be checked every 6 months for a period of 2 years after the placement of the two types of crowns . During these four control visits, primary and secondary outcomes will be assessed clinically and radiographically. The primary outcome is the success of the treatment defined by the absence of major failure. A composite measure of signs and symptoms leading to diagnosis of irreversible pulpitis or periradicular periodontitis will be used to define major failure (pain, pulp infection, dental abscess, periradicular pathology visible on radiograph). The secondary outcomes are parental and child satisfaction (size, form and color), retention and fracture of the PPC, the wear of the antagonist tooth, the gingival state near PPC using the indices Löe and Silness to record plaque index (PI), gingival index (GI) and depth of the pocket (DI) on the crowned tooth and the two adjacent ones. Each center has a trained and / or calibrated operator and evaluator.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tooth Decay

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Split mouth design
Masking
None (Open Label)
Allocation
Randomized
Enrollment
101 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PPC m
Arm Type
Active Comparator
Arm Title
PPC z
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
PPC z
Intervention Description
Installation of a preformed pediatric zircona crown
Intervention Type
Device
Intervention Name(s)
PPC m
Intervention Description
Installation of a preformed pediatric metal crown
Primary Outcome Measure Information:
Title
clinical and radiographique observations
Description
Success of the treatment defined by the absence of major failure. A composite measure of signs and symptoms leading to diagnosis of irreversible pulpitis or periradicular periodontitis will be used to define major failure (pain, pulp infection, dental abscess, periradicular pathology visible on radiograph
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children of at least 4 years of good general health (ASAI or II), Child with at least two temporary molars of the same type, 1st or 2nd molar, contralateral (fractional mouth), meeting the following criteria: The two temporary molars are affected by a cavitary carious lesion or a hypoplastic defect of at least 2 faces, the two temporary molars of the pair (54-64, 55-65, 74-84 or 75-85), should or should not be subjected to pulpotomy prior to the realization of the CPP, the two molars must have an antagonistic tooth. Consent of parents (legal guardians) and child, Child and parents (legal guardians) speaking French, Child covered by his parents' social security cover, Child cooperating in the vigilant or sedated state (cooperation evaluated with a Venham score 0, 1, 2). Exclusion Criteria: Child who does not cooperate in care under vigil or under conscious sedation, who must therefore be treated under general anesthesia. Child allergic to local anesthetics, chromium or nickel. Exclusion dental criteria Primary molar whose physiological exfoliation will appear within 24 months or pimary molar with a root resorption of more than a third of the radicular length. Severely decayed PM prohibiting the retention and the sealing of the restoration. Primary molar with exposed cement or with evidence of swelling in the surrounding tissues Molar with spontaneous pain. Primary molar in infraclusion. Primary molar whose radiographic examination reveals a widening of the desmodontal space, the presence of radiolucent image on the root furcation and/or apices, internal or external resorption
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michele MULLER BOLLA
Phone
33 4 92 03 32 70
Email
michele.muller@unice.fr
First Name & Middle Initial & Last Name or Official Title & Degree
mélanie bonnard
Email
bonnard.m@chu-nice.fr
Facility Information:
Facility Name
CHRU Lille
City
Lille
ZIP/Postal Code
59000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Caroline DELFOSSE
Email
caroline.delfosse@univ-lille.fr
First Name & Middle Initial & Last Name & Degree
Caroline DELFOSSE
Facility Name
CHU de Nantes
City
Nantes
ZIP/Postal Code
44000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
serena LOPEZ CAZAUX
Email
serena.lopezcazaux@gmail.com
First Name & Middle Initial & Last Name & Degree
Serena LOPEZ CAZAUX
Facility Name
CHU de Nice
City
Nice
ZIP/Postal Code
06000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michele MULLER BOLLA
Email
muller@unice.fr
Facility Name
CHU Stransbourg
City
Strasbourg
ZIP/Postal Code
67000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
françois CLAUSS
Email
francois_clauss@hotmail.com
First Name & Middle Initial & Last Name & Degree
françois CLAUSS

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31445509
Citation
Lopez-Cazaux S, Aiem E, Velly AM, Muller-Bolla M. Preformed pediatric zirconia crown versus preformed pediatric metal crown: study protocol for a randomized clinical trial. Trials. 2019 Aug 24;20(1):530. doi: 10.1186/s13063-019-3559-1.
Results Reference
derived

Learn more about this trial

Preformed Pediatric Crown Zirconia Versus Preformed Pediatric Metal Crown

We'll reach out to this number within 24 hrs