Manual and Rotatory Instrumentation Pulpectomy in Primary Mandibular Molars (RotaPulp)

December 8, 2020 updated by: Jaime Daniel Mondragón Uribe, Universidad de Guanajuato

Comparison Between Manual and Rotatory Instrumentation Pulpectomy Treatments in Primary Mandibular Molars

In this study, the aim is to compare manual and rotatory pulpectomy techniques on 100 primary mandibular molars on children between the ages of 4 and 8 years. The plan is to conduct a randomized controlled trial with a 1:1 ratio for group allocation at a teaching university pediatric dentistry clinic between January 2021 and December 2021. Two manual systems, as well as two rotary systems, will be randomly assigned. The adult manual system used will be K-file and the adult rotary system will be K3. The pediatric manual system used in this study will be Kedo-SH, while the pediatric rotary system will be Kedo-S. The observed outcome measures in this study are the following: 1) instrumentation and filling time; 2) filling quality by radiographic evaluation; 3) postoperative pain levels using the visual analog scale at 12 and 24 hours; and 4) frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Introduction

Dental caries is a prevalent chronic disease, affecting 60-90% of school-age children in industrialized countries; although in the last four decades the prevalence and severity of caries lesions have decreased, it is still a frequent disease for this age group. The American Dental Association (ADA) classifies dental caries by clinical presentation as initial, moderate, and severe; furthermore, the ADA classifies the disease using the international caries detection and diagnosis system (ICDAS II; International Caries Detection and Assessment System II) and by a radiographic presentation of the proximal faces based on the E0-E2, D1-D3 notation system. Within the non-vital pulp treatments, pulpectomy is indicated in temporary teeth; pulpectomy is a conventional endodontic treatment for teeth with exposed, infected, and/or necrotic tissue to eliminate pulp and periradicular infection.

In a recent systematic review that compared three different strategies for the management of deep caries lesions (i.e. complete caries removal, selective caries removal, and step caries removal), Aïem and colleagues (2020) report an increased restoration failure risk when selective removal is used compared to complete removal of caries. In a study where French dentists were surveyed on the management of deep caries lesions in primary dentition, the majority of respondents mentioned performing deep caries removal in a single step. Endodontic procedures in the pediatric population can assist to keep temporary teeth until exfoliation, which is a key principle of pediatric dentistry. Vital pulp and non-vital pulp treatments are employed in the treatment of severe lesions and deep caries; meanwhile, pulpectomy is a treatment largely used in the primary dentition. In pulp therapy, a pulpotomy is performed by removing the pulp from the chamber, while in a pulpectomy, all the tissue from both the chamber and the root canals is removed.

There are two parameters used to determine root canal treatment success: 1) the morphology and shaping of the canal; and 2) the duct cleanliness or the adequate level of disinfection provided by the type and quantity of intra-canal irrigation (e.g. chlorhexidine, sodium hypochlorite, citric acid, profuse irrigation). A pulpectomy is the technique of choice for primary dentition in deep carious lesions with pulp necrosis since pulpectomy has a higher success rate than pulpotomy. While the time for access to the root canal is less with the use of rotary instrumentation systems compared to a manual technique, manual techniques have the same efficacy as rotary systems in root canal cleaning procedures. Rotary systems have greater clinical success compared to manual techniques, in addition to having advantages in instrumentation time, canal shaping, reduction in working time, better cooperation and less patient fatigue, improvement in the conicity of the root canal, and promoting a higher quality of obturation. In a recent meta-analysis, Manchanda and colleagues (2020) conclude that rotary instrumentation has similar clinical and radiographic success rates to manual techniques in primary dentition; additionally, rotatory techniques show lower levels of postoperative pain and less instrumentation time. In the only study in the Mexican population that compared a rotary system (i.e. K3) against a manual technique (i.e. K-file) it was found that the instrumentation and obturation time was shorter, being a promising technique in children.

Given the limited comparative literature about rotatory techniques used in pulpectomy treatment, it is necessary to conduct clinical trials that compare both manual and rotatory techniques in first dentition treatment. So far, studies have been carried out comparing rotary systems designed for adults in the pediatric population. Recently, interest to validate and implement safe and effective protocols for the management of rotary systems in primary dentition has emerged in pediatric dentistry. Below is a protocol designed to investigate the advantages and disadvantages associated with the use of rotary systems designed for our population of interest.

Study design

Population: patients with pulpectomy indication according to the criteria mentioned by Kuo and colleagues (2006).

Place: Pediatric Dentistry Clinic, Universidad Latinoamericana, Campus Valle.

Time frame: January 2021 - December 2021

Sampling technique: convenience sampling with group randomization.

Study groups: 4 (n= 100 teeth)

  1. Patients who are treated with a manual pulpectomy and a K-file system.
  2. Patients who are treated with a manual pulpectomy and a Kedo-SH system.
  3. Patients who are treated with a rotatory technique pulpectomy and a K3 system.
  4. Patients who are treated with a rotatory technique pulpectomy and a Kedo-S system.

PICOS framework

P: pediatric population

I: manual system pulpectomy

C: rotary system pulpectomy

O: instrumentation and obturation time, filling quality by radiographic evaluation, postoperative pain levels at 12hr and 24hr, frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up.

S: a randomized controlled trial

Research question

Are there differences between the use of a manual system compared to a rotary system in the pediatric population?

Main objective

Compare the performance between a manual technique and a rotatory technique during biomechanical work.

Particular objectives

  1. Compare the instrumentation (i.e. during biomechanical work) and filling time between a manual technique and a rotatory technique.
  2. Compare the filling quality by radiographic evaluation between a manual technique and a rotatory technique at the end of the procedure.
  3. Compare postoperative pain levels using the visual analog scale at 12 and 24 hours.
  4. Compare the frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up between the two techniques.

Hypotheses

H1: The rotatory techniques will take less instrumentation and obturation time than the manual techniques.

H1: The quality of the obturation in the rotatory technique will be reported radiographically more frequently as optimal than the manual technique.

H1: The pain levels reported by patients will be lower in the rotatory technique than in the manual technique.

H1: The rotatory technique will have a lower frequency of complications such as fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency at each time point compared to the manual technique.

Statistical analysis

Descriptive statistics will be performed on all variables. Statistical analysis will be performed using SPSS 25 (SPSS Inc., Chicago, IL). All variables will be examined to determine the existence of outliers and whether or not they meet the Gaussian distribution assumption; furthermore, Gaussian distribution will be determined with the Shapiro-Wilk test and by visualizing the data through histograms and Q-Q graphs. The demographic and clinical variables will be summarized in proportions and percentages. Nominal variables will be evaluated with Chi-square tests to assess differences between groups. Categorical variables will be evaluated to determine statistical inferences with the Mann-Whitney test. Continuous variables will be assessed for statistical inferences using t-tests and Levene's test to assess variance equality. Statistical significance will be set at p= 0.05 and a Bonferroni correction will be made for multiple comparisons.

Sample size

The sample size necessary to detect statistically significant differences was calculated by taking the following parameters; α = 0.05 and statistical power of 0.8 (i.e. 1-β). For the calculation of the sample size, the time of instrumentation was used as a measure of clinical outcome. The sample was calculated based on the article by Ochoa-Romero and colleagues (2011) where instrumentation time was used as the primary outcome. The sample calculator used can be found on the website: https://clincalc.com/stats/samplesize.aspx. The calculator designed for two independent groups for continuous variables was selected, using the mean for each group (i.e. group 1: rotatory technique 1.7 minutes ± 0.5; group 2: manual technique 2.5 minutes ± 0.8) taking into account an enrollment 1:1 ratio for this study. The total sample size was 24 teeth (i.e. at least 6 teeth per group to find statistically significant differences in instrumentation time).

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Not Applicable

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

  • Mexico
      • Mexico City, Mexico, 03100
        • Recruiting
        • Clínica de Odontopediatría
        • Contact:
        • Contact:
        • Sub-Investigator:
          • Paola M Torres-Olivares, DDS
        • Sub-Investigator:
          • Nahiely Hernández-Espinoza, DDS
        • Sub-Investigator:
          • José A Almeida-Díaz, DDS
        • Sub-Investigator:
          • Thalia Palacios-Piedra, DDS
        • Sub-Investigator:
          • Matilde Z López-Rivera, DDS

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

4 years to 8 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Patients between 4 to 8 years old.
  2. Both genders.
  3. Patients with an indication for pulpectomy for mandibular molars, based on the of Kuo and colleagues criteria (2006).
  4. Patients requiring pulpectomy in posterior teeth.
  5. Adequate dental structure of the crown.
  6. Patients with a remnant structure of at least two-thirds of the root.
  7. Patients with a medical file at the Pediatric Dentistry Clinic, Universidad Latinoamericana, Campus Valle.
  8. Patients with signed informed consent.

Exclusion Criteria:

  1. Patients requiring pulpotomy, extraction, or pulp regeneration therapy.
  2. Patients who are older than 9 years.
  3. An unrestorable tooth.
  4. Internal resorption in the roots visible on radiographs.
  5. Teeth with mechanical or carious perforations of the floor of the pulp chamber.
  6. Excessive pathologic root resorption involving more than a third of the root.
  7. Excessive pathologic loss of bone support, with loss of the normal periodontal attachment.
  8. Presence of a dentigerous or follicular cyst.
  9. Periapical or interradicular lesion involving the crypt of the developing permanent successor.
  10. Patients with the diagnosis of molar incisor hypomineralization (MIH).
  11. Patient's whose legal guardian does not provide their informed consent to participate in this study.
  12. Uncooperative patients.

Elimination criteria

a. Patients who do not complete the treatment or radiographic follow-up at least at a cut-off point.

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Adult manual instrumentation
Primary mandibular molars who are treated with a manual pulpectomy and a K-file system.
Procedure: Manual pulpectomy
Primary mandibular molars treated with a manual pulpectomy and a K-file system or a Kedo-SH system.
Experimental: Pediatric manual instrumentation
Primary mandibular molars treated with a manual pulpectomy and a Kedo-SH system.
Procedure: Manual pulpectomy
Primary mandibular molars treated with a manual pulpectomy and a K-file system or a Kedo-SH system.
Active Comparator: Adult rotatory instrumentation
Primary mandibular molars treated with a rotatory technique pulpectomy and a K3 system.
Procedure: Rotatory technique pulpectomy
Primary mandibular molars treated with a rotatory technique pulpectomy and a K3 system or a Kedo-S system.
Experimental: Pediatric rotatory instrumentation
Primary mandibular molars treated with a rotatory technique pulpectomy and a Kedo-S system
Procedure: Rotatory technique pulpectomy
Primary mandibular molars treated with a rotatory technique pulpectomy and a K3 system or a Kedo-S system.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Instrumentation time
Time Frame: Minutes; intraoperative time.
The time needed to shape the root canal.
Minutes; intraoperative time.
Obturation time
Time Frame: Minutes, intraoperative time.
Time needed to obturate the root canals.
Minutes, intraoperative time.
Filling quality
Time Frame: Immediately after surgical procedure.
Radiographic evaluation of the root canal filling.
Immediately after surgical procedure.
Postoperative pain
Time Frame: 12 hours
Pain resulting from the surgical procedure, evaluated with the visual analog pain scale (range, 1 to 10; the higher the score the worst the outcome).
12 hours
Postoperative pain
Time Frame: 24 hours
Pain resulting from the surgical procedure, evaluated with the visual analog pain scale (range, 1 to 10; the higher the score the worst the outcome).
24 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Complications secondary to procedure
Time Frame: 3-months
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
3-months
Complications secondary to procedure
Time Frame: 6-months
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
6-months
Complications secondary to procedure
Time Frame: 9-months
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
9-months
Complications secondary to procedure
Time Frame: 12-months
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
12-months

Collaborators and Investigators

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

Sponsor

Universidad de Guanajuato

Collaborators

University Medical Center Groningen
Universidad Latinoamericana

Investigators

  • Principal Investigator: Benjamín Franco Sánchez, DDS, Universidad Latinoamericana
  • Principal Investigator: Marianela Hernández-Baños, DDS, Universidad Latinoamericana
  • Principal Investigator: Jaime D Mondragon, MD, MSc, University Medical Center Groningen, Universidad de Guanajuato

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

December 8, 2020

Primary Completion (Anticipated)

December 15, 2021

Study Completion (Anticipated)

July 15, 2022

Study Registration Dates

First Submitted

November 10, 2020

First Submitted That Met QC Criteria

November 18, 2020

First Posted (Actual)

November 19, 2020

Study Record Updates

Last Update Posted (Actual)

December 10, 2020

Last Update Submitted That Met QC Criteria

December 8, 2020

Last Verified

December 1, 2020

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ULA-2020-ODP-1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

All anonymized patient data will be made available upon request.

IPD Sharing Time Frame

At the conclusion of the study.

IPD Sharing Access Criteria

Access granted by the principal investigators.

IPD Sharing Supporting Information Type

  • Study Protocol
  • Statistical Analysis Plan (SAP)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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