RECRUITING

A Comparative Study of Hall Technique, Modified Hall Technique and Conventional Stainless-Steel Crown Restorations in the Treatment of Primary Molars With Proximal Caries Lesions.

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to compare the effectiveness of the Hall technique and modified Hall technique to the conventional Stainless-Steel Crown restoration in the treatment of primary molars with dentinal caries with or without proximal ridge intact.

Official Title

A Comparative Study of Hall Technique, Modified Hall Technique and Conventional Stainless-Steel Crown Restorations in the Treatment of Primary Molars With Proximal Caries Lesions.

Quick Facts

Study Start:2023-06-01
Study Completion:2025-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04822233

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:5 Years to 8 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Medically fit children
  2. * Children who exhibit cooperative behavior at initial bitewing radiograph procedure
  3. * Children with symptom-free or reversible pulpitis restorable first and second primary molars in both arches
  4. * Teeth with D1 lesions will be included
  5. * No periapical or furcation pathologies on bite wing radiographs
  1. * Medically compromised children
  2. * Children with uncooperative behavior during bitewing radiograph process
  3. * Primary molars with irreversible pulpitis
  4. * Teeth with furcation or peri radicular pathologies

Contacts and Locations

Study Contact

Nathanael O Salako, BDS,MSc
CONTACT
(713) 486-4141
Nathanael.O.Salako@uth.tmc.edu
Sandra Jung
CONTACT
713-486-4026
Sandra.Jung@uth.tmc.edu

Principal Investigator

Nathanael O Salako, BDS,MSc
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Nathanael O Salako, BDS,MSc, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-01
Study Completion Date2025-12-01

Study Record Updates

Study Start Date2023-06-01
Study Completion Date2025-12-01

Terms related to this study

Keywords Provided by Researchers

  • molars

Additional Relevant MeSH Terms

  • Dental Caries