Effect of Different Root Canal Instruments on Removal of Endotoxins From Necrotic Root Canals
Primary Purpose
Endodontic Disease
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
one shape
protaper next
Sponsored by
About this trial
This is an interventional other trial for Endodontic Disease focused on measuring rotary instruments, endotoxins
Eligibility Criteria
Inclusion Criteria:
- Patients who are medically free and good health.
- Patient 's age between 20-60years.
- Patients with posterior teeth diagnosed clinically and confirmed by thermal sensitivity tests as teeth with necrotic pulp.
- Positive patient's acceptance for participation in the study.
Exclusion Criteria:
- -Pregnancy or lactation
- Medically compromised patients -Patients aged less than20 or more than 60 years.-
- Patients unable to give informed consent.
- Previous endodontic therapy of the affected tooth .
- Teeth diagnosed with vital pulp.
- Teeth with periodontal pocket more than 3mm deep.
- Teeth with abnormal anatomy and calcified canals.
- Teeth with caries below the bony level (non-restorable tooth).
- Teeth with periapical swelling or sinus tract.
Sites / Locations
- Cairo University Faculty of Dentistry
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
one shape
protaper next
Arm Description
single file rotary system
multiple file rotary system
Outcomes
Primary Outcome Measures
endotoxin change
Human endotoxin (ET) ELISA Kit will be used to measure endotoxin concentrations in the root canals before and after chemomechanical procedures.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03641612
Brief Title
Effect of Different Root Canal Instruments on Removal of Endotoxins From Necrotic Root Canals
Official Title
Effect of Different Root Canal Instruments on Removal of Endotoxins From Necrotic Root Canals (A Randomized Clinical Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
August 10, 2018 (Actual)
Primary Completion Date
November 1, 2018 (Actual)
Study Completion Date
November 10, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Heba Elasfouri
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
• Grouping: The patients will be randomly assigned into two equal groups Group : OneShape Group: ProtaperNext
Endodontics procedure steps:
Patient will be anesthetized by using infiltration local anesthesia or nerve block according to the tooth location in mandibular or maxillary arch respectively.
All caries will be removed, then isolation using rubber dam, the crown and surrounding structures will be disinfected with 30% H2O2( hydrogen peroxide) for 30 seconds, followed by 2.5% NaOCl for the same period of time and then inactivated with 5% sodium thiosulphate.
2- For the access cavity preparation, a sterile/apyrogenic high-speed diamond bur will be used in conjunction with manual irrigation with sterile saline. Before entering the pulp chamber, the access cavity will be disinfected according to the protocol described above.
2- Root canal length will be determined, by preoperative radiograph then (S1) will be taken by introducing a sterile/apyrogenic paper point #15/ 20 (5paper points) into the full length of the canal and left there for 1 minute. Then, the sample will be placed in an apyrogenic glass and stored in -20°. Then canal length will be confirmed by apex locator.
3- Cleaning and shaping will be done using either One shape or Protaper next rotary instruments in crown down preparation technique with the use of in an endodontic motor according to the manufacturer instructions, the canals will be thoroughly irrigated using 3ml of 2.5% Sodium hypochlorite between every subsequent instrument.
4-After root canal preparation, NaOCl will be inactivated with 5 mL of sterile 5% sodium thiosulphate for 1 minute, which then will be removed with 5 mL of sterile/apyrogenic saline solution., which then will be removed with 5 mL of sterile/apyrogenic saline solution. second endotoxin sample (S2) will be taken from the root canals. (5 paper point size of the master cone).
5- After completion of instrumentation and irrigation, obturation will be done using size 30/ 0.4 taper gutta-percha cones and auxiliaries as needed using the modified single cone technique.
Determination of Endotoxin Concentration Human endotoxin (ET) ELISA Kit will be used to measure endotoxin concentrations in the root canals before and after chemomechanical procedures.
Detailed Description
Materials and Methods:
A. Trial Design:
The trial design of this study will be a prospective, parallel, Randomized clinical trial (RCT). The clinical trial involves research using human participants. In this trial, the participants will be randomly allocated to receive one of two interventions according to the protocol created by the investigator; one of these interventions will be the control. The investigator is to determine the safety and/or the efficacy of the interventions after being received by the participants by measuring the outcomes because the outcomes will be measured, RCTs are quantitative studies.
• Grouping: The patients will be randomly assigned into two equal groups according to the type of rotary endodontic system used during root canal preparation: Group : OneShape Group : ProtaperNext
Endodontics procedure steps:
Patient will be anesthetized by using infiltration local anesthesia or nerve block according to the tooth location in mandibular or maxillary arch respectively.
All caries will be removed, then isolation using rubber dam, the crown and surrounding structures will be disinfected with 30% H2O2 ( hydrogen peroxide) for 30 seconds, followed by 2.5% NaOCl for the same period of time and then inactivated with 5% sodium thiosulphate.
2- For the access cavity preparation, a sterile/apyrogenic high-speed diamond bur will be used in conjunction with manual irrigation with sterile saline. Before entering the pulp chamber, the access cavity will be disinfected according to the protocol described above.
2- Root canal length will be determined, by preoperative radiograph then (S1) will be taken by introducing a sterile/apyrogenic paper point #15/ 20 (5paper points) into the full length of the canal and left there for 1 minute. Then, the sample will be placed in an apyrogenic glass and stored in -20°. Then canal length will be confirmed by apex locator.
3- Cleaning and shaping will be done using either One shape or Protaper next rotary instruments in crown down preparation technique with the use of in an endodontic motor according to the manufacturer instructions, the canals will be thoroughly irrigated using 3ml of 2.5% Sodium hypochlorite between every subsequent instrument.
4-After root canal preparation, NaOCl will be inactivated with 5 mL of sterile 5% sodium thiosulphate for 1 minute, which then will be removed with 5 mL of sterile/apyrogenic saline solution., which then will be removed with 5 mL of sterile/apyrogenic saline solution. second endotoxin sample (S2) will be taken from the root canals. (5 paper point size of the master cone).
5- After completion of instrumentation and irrigation, obturation will be done using size 30/ 0.4 taper gutta-percha cones and auxiliaries as needed using the modified single cone technique.
6- All procedures will be done in a single-visit, checked radiographically and recorded in the procedure chart.
Determination of Endotoxin Concentration Human endotoxin (ET) ELISA Kit will be used to measure endotoxin concentrations in the root canals before and after chemomechanical procedures.
As a parameter for calculation of the amount of endotoxins in the root canal samples, a standard curve will be plotted by using the endotoxin of known concentration supplied by the kit according to the manufacturer's instructions.
The test procedure will be performed according to the manufacturer's instructions. And the absorbance of endotoxins will be measured by using spectrophotometer at wavelength 450 nm.
D. Outcomes:
Evaluation of the antibacterial effect of using One Shape and Protaper Next rotary endodontic NiTi instruments for root canal preparation using Human endotoxin (ET) ELISA Kit
E. Randomization:
The randomization will be done in three steps:
Sequence generation:
The random sequence generation will be done for the patients' numbers (from 1 to 38) using Microsoft Excel software.
Allocation concealment mechanism:
The allocation concealment will be phone-based.
Implementation:
The random sequence will be done by a colleague and the random sequence table will be kept with him. After eligibility assessment, the operator would call the colleague for eligibility checking and to know the group assignment for the patients.
F. Blinding:
Participants, outcome assessor and data analyst will be blinded in this trial. The operator will be not blinded.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endodontic Disease
Keywords
rotary instruments, endotoxins
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The trial design of this study will be a prospective, parallel, Randomized clinical trial (RCT).
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
one shape
Arm Type
Experimental
Arm Description
single file rotary system
Arm Title
protaper next
Arm Type
Active Comparator
Arm Description
multiple file rotary system
Intervention Type
Other
Intervention Name(s)
one shape
Intervention Description
canal fluid sample before and after root canal instrumentation
Intervention Type
Other
Intervention Name(s)
protaper next
Intervention Description
canal fluid sample before and after root canal instrumentation
Primary Outcome Measure Information:
Title
endotoxin change
Description
Human endotoxin (ET) ELISA Kit will be used to measure endotoxin concentrations in the root canals before and after chemomechanical procedures.
Time Frame
Samples will be collected before and after chemomechanical preparation over 2 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients who are medically free and good health.
Patient 's age between 20-60years.
Patients with posterior teeth diagnosed clinically and confirmed by thermal sensitivity tests as teeth with necrotic pulp.
Positive patient's acceptance for participation in the study.
Exclusion Criteria:
-Pregnancy or lactation
Medically compromised patients -Patients aged less than20 or more than 60 years.-
Patients unable to give informed consent.
Previous endodontic therapy of the affected tooth .
Teeth diagnosed with vital pulp.
Teeth with periodontal pocket more than 3mm deep.
Teeth with abnormal anatomy and calcified canals.
Teeth with caries below the bony level (non-restorable tooth).
Teeth with periapical swelling or sinus tract.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
heba elasfouri, lecturer
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
marwa bedier, lecturer
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cairo University Faculty of Dentistry
City
Cairo
Country
Egypt
12. IPD Sharing Statement
Learn more about this trial
Effect of Different Root Canal Instruments on Removal of Endotoxins From Necrotic Root Canals
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