- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04793308
Radicular Dentin Remaining, Risk of Perforation and Canal Transportation in Manual Versus Rotary Instrumentation in Primary Molars
Comparison of Radicular Dentin Remaining, Risk of Perforation and Canal Transportation Between Manual Versus Rotary Instrumentation in Root Canals of Extracted Second Primary Molars: In Vitro Study
Study Overview
Detailed Description
Aim of the study:
To compare the shape & diameter of root canals, risk of perforation and the canal transportation after using rotary versus manual instruments on root extracted second primary molars.
Methodology:
Extracted second primary molars will be collected from the dental clinics of Pediatric Dentistry and Dental Public Health Department, Faculty of Dentistry, Cairo University.
The teeth are extracted either due to periodontal problems or because they are not restorable (beyond restoration) by the conventional coronal restorations or full coverage restorations in the case of root caries.
The teeth will be selected according to our inclusions and exclusion criteria. The teeth will be collected, sterilized and stored according to the Occupational Safety and Health Administration guidelines and regulations, ultrasonic scaler will be used to clean and remove soft tissue debris and calculus attached to the teeth.
Teeth will be divided into two groups:
Group (1); ((ProTaper Next, Rotary system). Group (2); K- files, Manual instruments. For cleaning and shaping of the canal system and mechanical preparation of root canal treatment.
Then shape of the canal (Canal transportation), canal diameter and risk of canal perforation will be compared in both groups.
Before and after preparation of the root canal, the shape of the canal will be assessed by using cone-beam computed tomography (CBCT) and diameter of the canal will be measured by using cone-beam computed tomography (CBCT).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Cairo, Egypt, 0022
- Department of Pediatric Dentistry, Faculty of Dentistry, Cairo University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Extracted Second primary molars. Extracted second primary molars with at least 2/3 of root remaining or with minimal apical resorption.
Extracted second primary molars without visual perforation resorption.
Exclusion Criteria:
- Exfoliated second primary molars. If pre assessment radiograph for extracted second primary molars reveals internal or external root resorption.
Extracted second primary molars with extreme root curvature.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group (1); (ProTaper Next, Rotary system).
Group I teeth were prepared with rotary instrumentation using ProTaper Next (Dentsply, Switzerland)
|
Engine-driven nickel titanium Ni-Ti instruments
|
|
Experimental: Group (2); K- files, Manual instruments.
Group II root canals were prepared by manual instrumentation using K type files Mani, Japan).
|
Engine-driven nickel titanium Ni-Ti instruments
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Radicular dentin remaining
Time Frame: 3 months
|
Assessment of dentin remaining by Cone Beam Computerized Tomography (CBCT)
|
3 months
|
|
Transportation of Root Canal
Time Frame: 3 months
|
Assessment of Root Canal Transportation by Cone Beam Computerized Tomography
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Risk of Perforation
Time Frame: 3 months
|
By Cone Beam Computerized Tomography (CBCT)
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rania Nasr, Assoc. Prof., Cairo University
- Principal Investigator: Hany Sadek, Assoc. Prof., Cairo University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 111120
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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