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CompletedNCT06157021RCTUpdated Feb 11, 2026

Obturation Quality in Primary Molars

An interventional study of Rotary pulpectomy and Manual pulpectomy in Necrotic Primary Molars, sponsored by Cairo University. Completed at 1 site in Egypt. Open to participants aged 4 Years to 8 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-11.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
4 Years to 8 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Necrotic Primary Molars

Keywords

  • Rotary instrumentation
  • pulpectomy
  • primary molars
  • obturation quality
03

In context

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years to 8 Years
Sexes eligible
All
Accepts 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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    Rotary pulpectomy

    Rotary pulpectomy using rotary files (Fanta AF baby\* rotary files and Endo Radar\* rotary device

    Procedure: Rotary pulpectomy

  • Active comparator
    Manual pulpectomy

    Manual pulpectomy using manual H files, Mani\*)

    Procedure: Manual pulpectomy

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).

    Also known as: (Fanta AF baby* rotary files and Endo Radar* rotary device).

  • ProcedureManual pulpectomy

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

    Also known as: Manual H files, Mani*)

06

What researchers measure

Primary outcomes

  1. parental acceptance

    done 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)

    Time frame: Immediately after the intervention

Secondary outcomes

  1. obturation quality

    (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

    Time frame: Immediately after the intervention and after 6 months

07

Study locations

1 site
  • Faculty of Dentistry, Cairo university
    Cairo, 11553, Egypt
08

References and documents

Individual participant data

Plan to share: No — No plan to share

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06157021
Lead sponsor
Cairo University
Responsible party
Rasha Adel Ragab (Lecturer, Cairo University) — Principal investigator
First posted
Dec 5, 2023
Start date
Nov 15, 2023
Primary completion
Jun 15, 2024
Completion
Jul 15, 2024
Last update
Feb 11, 2026

Study contacts

Rasha A Ragab, Lecturer
principal investigator · Faculty of Dentistry, Cairo University, Egypt.

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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