An interventional study of Pediatric Rotary File Systems in Root Canal Treatment, sponsored by Ain Shams University. Status unknown. Open to participants aged 4 Years to 7 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-02-10.
Sponsored by Ain Shams University · Not applicable, Interventional, and Treatment
The aim of the current study is evaluation and comparsion between two different paediatric rotary file systems and Manual K-file both clinically and radiographically .This study consist of two parts:I-In vivo part (RCT) II-In vitro part
The in-vivo part:
Its sample size was found to be 30 primary molars (10 teeth for each group)
Group1: Kedo S plus file study group (The teeth will be instrumented by Kedo S plus file) Group2: Kidzo file study group (The teeth will be instrumented by Kidzo file) Group3: Manual K-file control group (The teeth will be instrumented by Manual K-file)
Pulpectomy of primary molars according the protocol of individual group will be made, after that the teeth will be evaluated Immediately for :
1-Instrumentation time 2-Quality of obturation and evaluated at 1, 3, 6, 12 months for clinical and radiographic success
The aim of the current study is to evaluation and comparsion between two different paediatric rotary file systems (Kedo S plus file and Kidzo File) and Manual K-file both clinically and radiographically
Primary Objective:
Evaluation of clinical success, instrumentation time and quality of obturation of two different paediatric rotary file systems and manual K-file system in pulpectomy in primary molars both clinically and radiographically (In-vivo part of the study).
Testing hypothesis:
The null hypothesis (H 0 ): there is no difference in clinical success, instrumentation time ,quality of obturation and apical debris extrusion between the two different pediatric rotary systems and manual K-file system in pulpectomy in primary molars
PICOTS:
P - Participants: Children in the age group of 4-7 years having pulpally involved Primary teeth indicated for pulpectomy, I - Intervention: Pulpectomy procedure in primary molars using Kedo S plus file and Kidzo file.
C - Comparison: Manual K-file.
O- Outcomes:
The predicted sample size was found to be 30 teeth (10 teeth per group) which was calculated by using G*Power version 3.1.9.7. Sample size will be increased by about 10% to compensate for the drop out.
Selection of primary molars, of 4 to 7 year old patients, following the inclusion criteria N=30
All Participant will be a randomly allocated into one of the either group (10 teeth in each group):
Group1: Kedo S plus file study group (The teeth will be instrumented by Kedo S plus file) Group2: Kidzo file study group (The teeth will be instrumented by Kidzo file) Group3: Manual K-file control group (The teeth will be instrumented by Manual K-file)
Pre-operative intraoral periapical radiograph for assessing the root structure and confirming the diagnosis of pulpal involvment
Pulpectomy of primary molars according the protocol of individual group
In this study, the following materials will be used:
Stainless Steel Crown Clinical procedure Group 1: (Kedo S plus file study group)
Group 2: (Kidzo-file study group) Steps 1-7 will be done as mentioned above. Then, Kidzo file will be used for instrumentation according to manufacturer's instructions. Step 9-14 also, will be repeated as well.
Group 3: (Manual K-file control group) Steps 1-7 will be done as mentioned above also. Then, the teeth will be instrumented by using hand k-files. Again step 9-14 will be repeated as well.
Outcome measurement
Immediate post operative
A-The instrumentation time:
Will be recorded using a digital stopwatch, which include only instrumentation time of the used files excluding the in-between irrigation protocol for assessing the accurate time period needed for instrumentation in each group.
B-The quality of obturation:
Will be assessed according to criteria of Coll and Sadrian (1996) as (Underfilled, Optimal filled or Overfilled) by using intraoral periapical radiograph by paralleling technique.
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Clinical and radiographic success The following table indicating to the clinical and radiographic Coll and Sadrian.
criteria for treatment success,(1996) (44) : Clinical criteria Radiographic criteria 1. Absence of pain on percussion on recall checkup 1. No pathologic root resorption 2. No gingival swelling or sinus tract 2. No widening of the periodontal ligament space 3. Absence of purulent exudate expressed from the gingival margin 3. Absence or decrease of any periapical or furcation involvement 4. No abnormal mobility of tooth
Ain Shams University is the lead sponsor of 1,876 studies on the registry; 423 are open to participants now.
Of its 32 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
parents who refuse to sign informed consent to participate in the study
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Group1: Kedo S plus file study group (The teeth will be instrumented by Kedo S plus file)
Device: Pediatric Rotary File Systems
Group2: Kidzo file study group (The teeth will be instrumented by Kidzo file)
Device: Pediatric Rotary File Systems
Group3: Manual K-file control group (The teeth will be instrumented by Manual K-file)
Device: Pediatric Rotary File Systems
* Kedo S plus (p1 molar file ) (A1 anterior file) * Kidzo-file system 25/4 30/4 30/6
clinical outcome through participant clinical examination
Evaluation of participants with clinical success according to Coll and Sadrian criteria for treatment success No pain, No sweeling , No exudate, No abnormal mobility
Time frame: from baseline to 12 months
The quality of obturation will be assessed by using periapical intra oral radiographic parallel technique
the quality of obturation will be assessed from the obtained x - ray film by visual examination to evaluate it under the following categories: Under filled- Optimal filled- Over filled
Time frame: from baseline to 12 months
Instrumentation time
time of instrumentation will be measured immediatly by digital watch in seconds
Time frame: immediatly after procedure
No study locations are listed for this record.
Plan to share: No
No publications or documents are linked to this record.
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Ain Shams University