The Effectiveness of Hyperpure Chlorine Dioxide and Sodium Hypochlorite Irrigants in Endodontic Retreament in RCT

NCT ID: NCT04954638

Last Updated: 2022-10-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-11-15

Study Completion Date

2025-07-31

Brief Summary

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Endodontic treatment aims to eliminate pathogenic microbes from the root canal. Hyperpure chlorine dioxide is an endodontic irrigant. Our goal is to compare the efficacy of hyperpure chlorine dioxide with the gold standard sodium hypochlorite in the non-surgical retreatment of root canal treated teeth with chronic periapical lesions in a randomized clinical trial. Forty patients having chronic apical periodontitis will randomly be chosen for the study from the patients attending our Department of Conservative Dentistry. Endodontic treatment will be done according to professional quidelines. The patients will randomly be divided into two groups. In the first (control) group sodium hypochlorite, in the second group hyperpure chlorine dioxide will be used as desinfectant. The first sample will be taken from the root canal after removing the previous root canal obturation prior to desinfection. The second sample will be taken one week after temporization. The samples will be evaluated by culturing, MALDI-ToF and PCR strip test. After root canal obturation the the periapical status will be followed by clinical evaluation and control x-rays.

Detailed Description

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Endodontic treatment aims to eliminate pathogenic microbes from the root canal. This is an almost impossible task as microbes, especially Enterococci are able to line the dentin tubules that are nearly unaccessable to desifectants used during treatment. Hyperpure chlorine dioxide is an endodontic irrigant. In vitro studies proved it to be a very potent desinfectant against which bacteria do not produce resistency. It selectively binds to three amino acids targeting bacterial cells. Due to its small molecular weight and its highly volatile characteristics we presume that it is able to penetrate into the small dentin tubuli. There have been many in vitro studies comparing its characteristics and efficacy, but there have been no in vivo studies done to approve its clinical preformance so far. Our goal is to compare the efficacy of hyperpure chlorine dioxide with the gold standard sodium hypochlorite in the non-surgical retreatment of root canal treated teeth with chronic periapical lesions in a randomized clinical trial. Its efficacy will be compared by microbiological methods and by clinical and radiological evaluation. According to our hypothesis hyperpure chlorine dioxide is more effective antimicrobial agent than the gold standard sodium hypochlorite. The protocol for this clinical study was approved by the Hungarian National Ethics Committee for clinical trials. Forty patients having chronic apical periodontitis will randomly be chosen for the study from the patients attending our Department of Conservative Dentistry. Written consent will be collected from the patients. Only those patients will be accepted who had the root canal treatment done more than four years ago, the tooth is asymptomatic, functionally and esthetically restorable, the coronal restoration can be done within 3-4 weeks of the root canal obturation, who will not have prosthetic or orthodontic treatment interfering with the radiological follow-up and have no general medical conditions or medication influencing the healing of the periapical lesion. Endodontic treatment will be done according to professional quidelines. After sterilizing the tooth and its environment, a sterility test will be be done by taking samples from the top of the restoration (S1) and from the pulp chamber (S2). The root canal obturation will be removed mechanically and a microbiological sample will be taken from the root canal (M1). After taking the sample from the root canal the tooth will be chemomechanically prepared. The patients will randomly be divided into two groups. In the first (control) group sodium hypochlorite, in the second group hyperpure chlorine dioxide will be used as desinfectant. The sample taking procedure will be repeated after one week of temporization (sterility tests S3, S4 and root canal sample M2). The samples will be cultured and identified by MALDI-ToF MS. The remaining samples will be used for PCR testing (Micro-IDent Plus11, Hain Lifescience) to determine the presence of the tested bacteria. In the second session the root canal obturation will be completed. Following coronal restoration a control x-ray will be done by using an individual bite-block for standardization. The success of the root canal treatment will be followed-up by evaluating the periapical status with the Periapical Index scoring system and clinical evaluation according to the criteria set by the European Society of Endodontology including pain assessment where the patients rate pain on the VNRS, with 0 = ''no pain'' to 10 = ''worst pain imaginable". Clinical evaluation and control x-rays will be done at 6 months, 1, 2, 3, and 4 years following treatment. The x-rays will be evaluated by two blinded calibrated examiners.

Conditions

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Persistent Infection Periapical Lesion

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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sodium hypochlorite

group 1: control group with sodium hypochlorite desinfection

endodontic desinfection

Intervention Type OTHER

* outcome assessment of the retreatment of endodontically treated teeth presenting chronic apical periodontitis
* effectiveness of hyperpure chlorine dioxide compared with sodium hypochloride
* using microbiological methods
* outcome assessed by radiological method and clinical evaluation

hyperpure chlorine dioxide

group 2: study group with hyperpure chlorine dioxide desinfection

endodontic desinfection

Intervention Type OTHER

* outcome assessment of the retreatment of endodontically treated teeth presenting chronic apical periodontitis
* effectiveness of hyperpure chlorine dioxide compared with sodium hypochloride
* using microbiological methods
* outcome assessed by radiological method and clinical evaluation

Interventions

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endodontic desinfection

* outcome assessment of the retreatment of endodontically treated teeth presenting chronic apical periodontitis
* effectiveness of hyperpure chlorine dioxide compared with sodium hypochloride
* using microbiological methods
* outcome assessed by radiological method and clinical evaluation

Intervention Type OTHER

Other Intervention Names

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hyperpure chlorine dioxide, sodium hypochlorite

Eligibility Criteria

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Inclusion Criteria

• patients having asymptomatic chronic apical periodontitis of size 4-5 according to periapical index scoring system

Exclusion Criteria

* patients who suffer from diabetes, osteoporosis, cancer, autoimmue disease
* patients who are in immune suppressed state
* patients receiving steroid, bisphosphonate, denosumab or antiangiogenic therapy
* alcoholism
* smoking
* patients having had antibiotic therapy in the past 4 weeks before starting treatment
* teeth with furcation involvement
* teeth with deeper than 4 mm probing depth or the same on neighboring teeth
* patients intending to undergo prosthodontic or orthodontic treatment within four years
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eniko Vaszine Szabo

OTHER

Sponsor Role lead

Responsible Party

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Eniko Vaszine Szabo

principal investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Enikő Vasziné Szabó, DMD PhD

Role: PRINCIPAL_INVESTIGATOR

Semmelweis University

Zsolt Lohinai, DMD PhD

Role: STUDY_DIRECTOR

Semmelweis University

Locations

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Semmelweis University, Dental Faculty, Conservative Dentistry Department

Budapest, , Hungary

Site Status

Countries

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Hungary

Other Identifiers

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OGYÉI/39205/2018

Identifier Type: -

Identifier Source: org_study_id

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