The Indications of First Molar Extraction at Tufts University, School of Dental Medicine

September 15, 2025 updated by: Bjorn Steffensen, Tufts University

The Indications of First Molar Extraction at Tufts University, School of Dental Medicine--A 14-year Retrospective Study

The aim of the present study is to investigate whether there has been a change of criteria for tooth extraction at Tufts University School of Dental Medicine (TUSDM) from 2005 to 2018. The primary outcome is the change of mean of radiographic interproximal bone loss of extracted teeth. The secondary outcomes are changes of other parameters (periodontal, endodontic and restorative) of extracted teeth and reasons for extraction.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

The purpose of the present study is to quantitatively evaluate the change in tooth extraction at school setting over the past 14 years.

Aims The aim of the present study is to investigate whether there has been a change of criteria for tooth extraction at Tufts University School of Dental Medicine (TUSDM) from 2005 to 2018. The primary outcome is the change of mean of radiographic interproximal bone loss of extracted teeth. The secondary outcomes are changes of other parameters (periodontal, endodontic and restorative) of extracted teeth and reasons for extraction.

Hypothesis Criteria for extraction of first molar teeth has changed between 2005 and 2018 toward early extraction of teeth with less severe periodontal and other conditions.

Significance Currently, there is not study presenting the quantified data for criteria change for tooth extraction. Also, determining whether to extract a tooth or not actually requires taking several clinical parameters into consideration. The present study will give clinicians a broad review of the change in clinical decision making for tooth extraction.

Materials and Methods Retrospective chart review among patients in TUSDM Pre-doctoral and Post-doctoral Group Practices The study setting is among patients who received dental treatments at TUSDM. The database will be retrospectively reviewed by patients' electronic records in TUSDM Postgraduate (PG) and Undergraduate (UG) clinics from 01/01/2005 till 12/31/2018.

Study Type

Observational

Enrollment (Estimated)

240

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Boston, Massachusetts, United States, 02111
        • Tufts University School of Dental Medicine

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.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Patients who had fully-erupted first molar extraction (tooth number #3 or #14 or #19 or #30) under CDT code of D7140 (Extraction, erupted tooth or exposed root) and D7210 (Extraction, erupted tooth requiring removal of bone and/or sectioning of tooth, and including elevation of mucoperiosteal flap if indicated) at TUSDM

Description

Part 1:

Inclusion Criteria:

  1. Patients who had fully-erupted first molar extraction (tooth number #3 or #14 or #19 or #30) under Code on Dental Procedures and Nomenclature (CDT) code of D7140 (Extraction, erupted tooth or exposed root) and D7210 (Extraction, erupted tooth requiring removal of bone and/or sectioning of tooth, and including elevation of mucoperiosteal flap if indicated) at TUSDM.
  2. The electronic records must include the following data:

    • Gender
    • Age
    • Comprehensive periodontal chart, including probing depth (PD), clinical attachment level (CAL), furcation involvement and mobility. The periodontal chart has to be recorded within 12 months before tooth extraction
    • Periapical radiograph and bite-wing radiographs of extracted tooth. The radiographs have to be taken within 12 months before tooth extraction
    • Reasons for tooth extraction

Part 2:

Inclusion Criteria:

  1. Patients who had:

    • Fully-erupted first and second molars (tooth number #2, #3, #14, #15, #18, #19, #30, #31) that were extracted under CDT codes D7140 (Extraction, erupted tooth or exposed root) or D7210 (Extraction, erupted tooth requiring removal of bone and/or sectioning of tooth, and including elevation of mucoperiosteal flap if indicated).
    • The same extracted tooth were replace with dental implant placement under CDT code D6010 (Surgical placement, endosteal implant) within 24 months after extraction.
  2. The electronic records must include the following data

    • Sex
    • Age
    • Dental records including:

      • Periapical radiograph of the tooth before extraction: the radiographs have to be taken within 12 months before tooth extraction, including one or more of probing depth (PD), clinical attachment level (CAL), furcation involvement and tooth mobility.

Exclusion Criteria (both parts):

  1. Absence of tooth distal to extracted tooth.

    a. Clinical decision for tooth extraction may be affected by tooth location. When the tooth is the distal abutment in the dentition, clinicians tend to keep the tooth even if the prognosis is compromised.

  2. Presence of dental implant adjacent to extracted tooth a. Clinical decision for tooth extraction may be affected by adjacent dental implants.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Part 1: Change in mean of radiographic interproximal bone loss of extracted teeth
Time Frame: 2005-2018
  • All the measurements are based on the following reference points projected onto the theoretical tooth long axis

    • Cemento-enamel junction (CEJ); if there is dental restoration or prosthesis on tooth making CEJ undetectable on the radiographs, the apical margin of dental restoration or prosthesis will be used as CEJ
    • The most apical points of mesial and distal interproximal bone height
    • The apex of root
  • The radiographic mesial and distal bone loss will be determined by the proportion of the distance between bone height to apex and the distance between CEJ to apex, projected on the tooth axis
  • The greater bone loss of the mesial and distal sides on radiographs will be used for further analysis
2005-2018
Part 2: Change of criteria for tooth extraction
Time Frame: 2007-2018

The aim for sub-project 2 represent an extension of the Aim for Subproject 1 outlined above. This sub-project will investigate whether there has been a change of criteria for tooth extraction at TUSDM from 2007 to 2018 specifically for and limited to molar teeth that were extracted and subsequently replaced with dental implants.

Criteria for extraction of first molar teeth has changed between 2007 and 2018 toward early extraction of teeth with less severe periodontal and other conditions.

2007-2018

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Bjorn Steffensen, DDS, MS, PhD, Tufts University School of Dental Medicine

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 Major Dates

Study Start (Actual)

March 19, 2020

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

June 30, 2028

Study Registration Dates

First Submitted

January 8, 2021

First Submitted That Met QC Criteria

January 8, 2021

First Posted (Actual)

January 12, 2021

Study Record Updates

Last Update Posted (Estimated)

September 19, 2025

Last Update Submitted That Met QC Criteria

September 15, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • STUDY00000314

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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