ART Compared to the Hall Technique for Management HSPM

Sponsor
Tishreen University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05816096
Collaborator
(none)
31
1
2
13.2
2.4

Study Details

Study Description

Brief Summary

Aims: Evaluation of treatment success on HSPM-affected molars after ART and Hall technique.

comparison of pain during treatment with ART and Hall technique in HSPM. comparison of child and parent satisfaction with restorations used by ART and Hall technique.

Design: A randomized, controlled, crossover clinical study including thirty children.

Condition or Disease Intervention/Treatment Phase
  • Combination Product: Hall technique
  • Combination Product: ART
N/A

Detailed Description

Background and Aims:
Despite the widespread prevalence of HSPM:

there are no comparative studies yet between ART and Hall technique in the restoration of HSPM.

there are no studies yet on the success of ART in the treatment of HSPM.

Design:

A randomized, controlled, crossover clinical study including thirty children Each child will apply both of ART and Hall technique to him.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
31 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
A randomized, controlled, crossover clinical study, comparison of ART and Hall Technique.A randomized, controlled, crossover clinical study, comparison of ART and Hall Technique.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Atraumatic Restoration Treatment Compared to the Hall Technique for Management Hypomineralization Second Primary Molars
Actual Study Start Date :
Mar 26, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: A (Hall Technique)

31 child will be treated by one performed metal crown using Hall technique on one of HSPM affected tooth. The correct size of SSC for tooth will be selected. Use the separating rubber if necessary. Dried the tooth and cemented the SSC by glass ionomer luting cement and used finger pressure to seat the crown and instructed the child to bite down on the SSC. Half of the total number of children will received performed metal crown at the first by divided them randomly to the two groups using the randomization table.

Combination Product: Hall technique
The child will be placed to them SSC on one of their HSPM affected teeth. Pain during treatment will be assessed using the FLACC scale and satisfaction the child and parent will be evaluated using likert scale after the treatment immediately and after one month and evaluate the success restoration adapted from Innes et al. after 3_6_9_12 month.
Other Names:
  • A
  • Experimental: B (ART)

    31 child will be treated by Bulk fill glass hybrid restorative system (Equia Forte HT®) using Atraumatic restoration treatment on one of HSPM affected tooth. Isolate the tooth by cotton rolls, remove the carious soft tissue using hand instrument excavators then condition the cavity with a polyacrylic acid solution 11.5% for 10 seconds. After washed and dried the cavity insert the GIC and protect it by Equia forte coat. Half of the total number of children will received ART at the first by divided them randomly to the two groups using the randomization table.

    Combination Product: ART
    The child will be restored to them one of their HSPM affected teeth by GIC. Pain during treatment will be assessed using the FLACC scale and satisfaction the child and parent will be evaluated using likert scale after the treatment immediately and after one month and evaluate the success restoration adapted from Innes et al. after 3_6_9_12 month.
    Other Names:
  • B
  • Outcome Measures

    Primary Outcome Measures

    1. Dental pain assessed by FLACC scale [During the placement of the restoration]

      Evaluated by outcome assessor using the faces, legs, activity, cry, consolability behavioral rating scale (FLACC scale) a behavioral pain assessment scale which has five criteria face, legs, activity, cry, consolability, which are each assigned a score of 0,1 or2. Total score of scale is summed in range 0 to10, where:0=relaxed and comfortable; 1-3=mild discomfort; 4-6=moderate pain; 7-10=severe pain.

    Secondary Outcome Measures

    1. Child Satisfaction with the restoration assessed by the Likert scale [Immediately after the placement of the restoration]

      Self-assessment by the children using Likert scale which is a psychometric scale has five responses (very satisfied, satisfied, neutral, unsatisfied, very unsatisfied)

    2. Parent Satisfaction with the restoration assessed by the Likert scale [Immediately after the placement of the restoration after asking the child]

      Self-assessment by the parent using Likert scale which is a psychometric scale has five responses (very satisfied, satisfied, neutral, unsatisfied, very unsatisfied)

    3. Child Satisfaction with the restoration assessed by the Likert scale [After one month from treatment]

      Self-assessment by the children using Likert scale which is a psychometric scale has five responses (very satisfied, satisfied, neutral, unsatisfied, very unsatisfied)

    4. Parent Satisfaction with the restoration assessed by the Likert scale [After one month from treatment after asking the child]

      Self-assessment by the parent using Likert scale which is a psychometric scale has a five responses (very satisfied, satisfied, neutral, unsatisfied, very unsatisfied)

    Other Outcome Measures

    1. Clinical success of restoration assessed by evaluation criteria for restoration assessments after 3 months [After 3 months from treatment]

      Evaluated by outcome assessor using evaluation criteria for restoration assessments which has three scores (success, minor failures, major failures) for ART and Hall technique.

    2. Radiological success of restoration assessed by Radiological success cireteria after 6 months [After 6 months from traetment]

      Evaluated by outcome assessor using Radiological success cireteria for restoration. where the case is considered successful radiologically when all signs of pulpal necrosis are absent.

    3. Clinical success of restoration assessed by evaluation criteria for restoration assessments after 6 months [After 6 months from treatment]

      Evaluated by outcome assessor using evaluation criteria for restoration assessments which has three scores (success, minor failures, major failures) for ART and Hall technique.

    4. Clinical success of restoration assessed by evaluation criteria for restoration assessments after 9 months [After 9 months from treatment]

      Evaluated by outcome assessor using evaluation criteria for restoration assessments which has three scores (success, minor failures, major failures) for ART and Hall technique.

    5. Clinical success of restoration assessed by evaluation criteria for restoration assessments after 12 months [After 12 months from treatment]

      Evaluated by outcome assessor using evaluation criteria for restoration assessments which has three scores (success, minor failures, major failures) for ART and Hall technique.

    6. Radiological success of restoration assessed by Radiological success cireteria after 12 months [After 12 months from treatment]

      Evaluated by outcome assessor using Radiological success cireteria for restoration. where the case is considered successful radiologically when all signs of pulpal necrosis are absent.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    3 Years to 11 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Absolute positive, positive or negative behavior according to the Frankel Scale.

    • Healthy, both physically and mentally.

    • Do not take medications that interfere with the assessment of pain within 24 hours prior to treatment.

    • A child with HSPM-affected primary second molars on the right and left side in one jaw.

    • The HSPM affected teeth from 2-6 degree in Ghanim scale.

    • Teeth with atypical carious lesions.

    • Teeth with post-eruption destroyed

    • The presence of a clear, intact dentinal bridge between the caries and pulp radially.

    Exclusion Criteria:
    • Allergy to the substances used in restoration.

    • Presence of general or developmental medical conditions.

    • Teeth with pulpitis inflammation or apical lesion or non-restorable.

    • Teeth closed to being replaced.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Tishreen University Latakia Syrian Arab Republic

    Sponsors and Collaborators

    • Tishreen University

    Investigators

    • Study Chair: Nabih Raslan, Dr, Tishreen University
    • Principal Investigator: Aya Adl, Dr, Tishreen University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Tishreen University
    ClinicalTrials.gov Identifier:
    NCT05816096
    Other Study ID Numbers:
    • Restoration for HSPM
    First Posted:
    Apr 18, 2023
    Last Update Posted:
    Apr 18, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Tishreen University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 18, 2023