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Obturation Quality in Primary Molars

Evaluation of Obturation Quality in Necrotic Primary Molars After Manual Versus Rotary Pulpectomy; a Randomized Clinical Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06157021
Acronym
RCT
Enrollment
40
Registered
2023-12-05
Start date
2023-11-15
Completion date
2024-07-15
Last updated
2026-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Necrotic Primary Molars

Keywords

Rotary instrumentation, pulpectomy, primary molars, obturation quality

Brief summary

Forty cases of necrotic primary molars in children aged 4-8 years were selected to compare the effect of manual versus rotary pulpectomy regarding parental acceptance and obturation quality.

Detailed description

The present study was performed in the Department of Pediatric Dentistry and Dental Public Health Department, Faculty of Dentistry, Cairo University, Egypt. Ethical approval was obtained from the Ethical Committee board of Faculty of Dentistry, Cairo University, Egypt. Written informed consent was taken from the legal guardian of each participating child willing to participate in the trial, prior to the start of the clinical procedure after explaining the whole procedure in a simple way. The consent form was written in Arabic. A sample of 40 primary mandibular second molars of children between 4 and 8 years of age indicated for pulpectomy participated in this double-blinded randomized controlled trial. Parallel allocation design was adopted for the intervention and control arms with allocation ration 1: 1 (i.e. 20 cases each). The sample size was calculated considering the previously published studies with 95% power in detecting the true statistical significance among the two groups. Control group one: Manual pulpectomy using) H files, Mani\*) Group two: Rotary pulpectomy using (Fanta baby\* rotary files and Endo Radar\* rotary device). Diagnosis: Diagnostic chart was filled with personal, medical and dental history. 1. Intra & extra oral examination was made with aid of mirror and probe to assess the clinical inclusion criteria. 2. Preoperative photographs were taken 3. Preoperative radiograph were examined Intervention: Patients were assigned into two groups; Group A (Experimental group) (using rotary files) 1. Pre-operative radiograph showing all roots and their apices. 2. Local anaesthetic (to enable use of rubber dam clamp). 3. Rubber dam isolation. 4. Removal of caries. 5. Removal of roof of pulp chamber. 6. Identify root canals. 7. Irrigate with concentrated sodium hypochlorite followed by normal saline (0.9%) 8. Estimate working lengths of root canals keeping 2 mm short of the radiographic apex. 9. Insert rotary files into canals and debride the canals lightly and gently. 10. Irrigate the root canals. 11. Dry canals with pre-measured paper points, keeping 2 mm from root apices. 12. Canals were dried with paper points, obturated by injecting Metapex. (Meta Biomed - Metapex Root Canal Filling Material) 13. Stainless steel crown was performed Group B (control group) (using manual files) All steps as that of group A were done except step (j) instead of it; a manual files were inserted into the canals for debridement lightly and gently. Randomization &Allocation concealment:- Sequence generation Simple randomization was done by computer software (www.random.com) for patient's assignment in each group. Blinding: Blinding to the child participants and legal guardian of each participating child, inter examiner and statistician. Statistical analysis: Categorical data were presented as frequencies (n) and percentages (%). Intergroup comparisons were done utilizing Fisher's exact test. while intragroup comparisons were done utilizing Cochran's Q tests followed by Dunn's post hoc test. Ordinal data were presented as median and interquartile range values and were analyzed using Mann-Whitney U test for intergroup comparisons. The significance level was set at p ≤ 0.05 for all tests. Statistical analysis was performed with ® SPSS® (SPSS Inc., IBM Corporation, New York, USA) Statistics Version 26 for Windows.

Interventions

PROCEDURERotary pulpectomy

Pulpectomy procedures by making cleaning and shaping of root canals of necrotic primary molars using (Fanta AF baby\* rotary files and Endo Radar\* rotary device).

Pulpectomy procedures by making cleaning and shaping of root canals of necrotic primary molars using Manual H files, Mani\*)

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Blinding to the child participants and legal guardian of each participating child, inter examiner and statistician. The operator and the child were blinded to the intervention from the beginning till finishing the procedure of caries removal and access cavity. Blinding cannot be done during root canal instrumentation because of visual differences between manual and rotary files.

Intervention model description

Randomized controlled parallel double blinded study

Eligibility

Sex/Gender
ALL
Age
4 Years to 8 Years
Healthy volunteers
Yes

Inclusion criteria

* Medically free children. * Age: 4-8 years * Primary molars with necrotic pulp, abscess or fistula. * Teeth which if lost possibility of space maintainer construction exists. * Pre-operative radiograph showing absence of root resorption more than one third of the root.

Exclusion criteria

* Vital primary teeth. * Teeth with inadequate tooth structure to support the rubber dam. * Expected shedding time within one year. * Peri-radicular involvement extending to the permanent tooth bud. * Excessive internal\& external root resorption, * Perforation of pulpal floor. * Extensive tooth mobility

Design outcomes

Primary

MeasureTime frameDescription
parental acceptanceImmediately after the interventiondone by the participating parents who ranked their acceptance to pulpectomy procedures on a five-point Likert scale, as follows: 1, strongly acceptable; 2, acceptable; 3, neutral; 4, unacceptable; and 5, strongly unacceptable. (Scores from 1-3 means better outcome)

Secondary

MeasureTime frameDescription
obturation qualityImmediately after the intervention and after 6 months(Postoperative radiograph was used to determine obturation quality as (secondary outcome) using Coll and Sadrian criteria (Coll and Sadrian, 1996) at baseline postoperatively and after 6 months. Coll and Sadrian criteria define the root canal obturation quality as optimal fill, underfill, or overfill. Underfill means that all the canals were filled 1 mm or more short of the apex, optimal fill means that one or more canals have filling material ending at radiographic apex, and overfill means any canal showing filling material outside the root. Optimum filled means better outcome

Countries

Egypt

Contacts

PRINCIPAL_INVESTIGATORRasha A Ragab, Lecturer

Faculty of Dentistry, Cairo University, Egypt.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026