Efficacy of Pediatric Rotary File System Versus Hand Instrumentation for Root Canal Preparation in Primary Teeth

Pulpitis Clinical Trial

Official title: Efficacy of Pediatric Rotary File System Versus Hand Instrumentation for Root Canal Preparation in Primary Teeth: An In Vivo and In Vitro Study

Status Completed

Clinical Trial Summary

The teeth were randomly allocated in two equal groups :

Control group (A):- included 20 mandibular primary molars in which pulpectomy were performed by hand instrumentation system using K- File from size 15 to size 35.

Experimental Group (B):- included 20 mandibular primary molars in which pulpectomy were performed by rotary system using Kedo-SG rotary file system according to manufacturer's instructions

Methods of Evaluation

Stage I :- During and after canal preparation:- The following parameters were evaluated for all cases in both groups:- A- The instrumentation and canal filling time were recorded for both groups using stopwatch. B- Radiographic assessment for filling were done immediately postoperative to record :-

1. Distance between the apex to filling level of the mesial and distal roots .

2. Obturation form

Stage II : Follow up :

The follow up were carried out by clinical and radiographic evaluation for all cases in both groups:-

The clinical evaluation were carried out at (0 base line = after 7 days ) then after 1 , 3 , 6 and 12 months .

Radiographic evaluation were performed immediately postoperative as (0 baseline ) after cementation of stainless steel crowns for assessment of filling quality. Radiographs will be used for comparison for consequent radiographs . Follow ups were performed after 6 and 12 months.

Clinical Trial Description

The planned study is a randomized clinical controlled trial including apparently healthy children who were selected from the patients attending the Out- Patient Clinic , Pediatric Dentistry Department, Faculty of Dentistry, Suez Canal University. Informed written consent were obtained from parents or guardians of the children after full explanation of clinical procedures and detailed treatment plan.

The teeth were randomly allocated in two equal groups :

Control group (A):- included 20 mandibular primary molars in which pulpectomy were performed by hand instrumentation system using K- File from size 15 to size 35.

Experimental Group (B):- included 20 mandibular primary molars in which pulpectomy were performed by rotary system using Kedo-SG rotary file system according to manufacturer's instructions

Clinical procedures :

1. Preoperative digital periapical radiograph were taken using standardized paralleling technique using XCP device .

2. Local anesthesia were administered to the patient.

3. The tooth were isolated using rubber dam .

4. Caries were removed by large spoon excavator.

5. The cavities were cleaned by thoroughly rinsing with chlorohexidine 0.2% .

6. Access cavity were done under constant water cooling and suction using high speed round bur No.330 .

7. Pulp chamber were completely deroofed .

8. No .10 size K file were used to determine patency of canals.

9. The working length were determined by apex locator & periapical radiograph.

10. Depending on the group allocation , the canal instrumentation were done by step back technique using K- file (Mani ) from size 15 to size 35 in quarter pull turn motion apically or by crown down technique using Kedo-SG file rotary system using endodontic motor.

11 - After each instrumentation , the canal were irrigated by 1% sodium hypochlorite .

12- The canal were dried with paper points( #30 &#35) 13- Then canal were filled with creamy mix of Zinc oxide & Egenol. 14-Zinc phosphate cement were placed over Zinc oxide & Egenol then finally restored by Stainless steel crown .

15-Postoperative digital periapical radiographs were taken using standardized paralleling technique using XCP device .

Methods of Evaluation

Stage I :- During and after canal preparation:- The following parameters were evaluated for all cases in both groups:- A- The instrumentation and canal filling time were recorded for both groups using stopwatch. B- Radiographic assessment for filling were done immediately postoperative to record :-

1. Distance between the apex to filling level of the mesial and distal roots .

2. Obturation form

Stage II : Follow up :

The follow up were carried out by clinical and radiographic evaluation for all cases in both groups:-

The clinical evaluation were carried out at (0 base line = after 7 days ) then after 1 , 3 , 6 and 12 months .

The following clinical criteria were evaluated: -

• Spontaneous pain as described by Oginin and Undoye ( 29)

• Sensitivity to percussion presence or absence.

• Tooth mobility presence or absence.

• Examination of any changes of the mucobuccal folds (presence or absence of swelling, sinus, draining fistula or abscess).

If the tooth exhibits any of above clinical features, the pulpectomy was considered a failure (F); otherwise, it was regarded as clinical success (S).

Radiographic evaluation were performed immediately postoperative as (0 baseline ) after cementation of stainless steel crowns for assessment of filling quality. Radiographs will be used for comparison for consequent radiographs . Follow ups were performed after 6 and 12 months.

The following radiographic criteria were evaluated :-

• Presence or absence of widening of apical periodontal membrane space .

• Presence or absence of furcation radioluency .

• Presence or absence of internal or external root resorption .

All patients were examined using standardized intra oral paralleling periapical direct digital radiographs using the rinn (XCP) periapical film holder and a long cone. Radiometric and radiodensitometric analysis of the radiographs were carried out using the software of Digora (2.5) system.

Dates of follow up visits were written on the patient 's recall card , parents were asked to call if any symptoms of pain or infection occurred at any time before recall visit .If there is any complications during follow up periods, different techniques of treatment were done according to the case. ;

Related Conditions & MeSH terms

• Pulpitis

• NCT number: NCT06152354
• Study type: Interventional
• Source: Suez Canal University
• Status: Completed
• Phase: N/A
• Start date: October 2, 2022
• Completion date: October 18, 2023