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Necrotic Primary MolarsRCTNCT06157021

Obturation Quality in Primary Molars

A study testing Rotary pulpectomy and Manual pulpectomy in people with Necrotic Primary Molars, run by Cairo University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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 more about this study

Who is it for?
Ages 4 to 8 yearsHealthy volunteers can take part
Conditions the study is for
Necrotic Primary Molars
What is being tested?
Rotary pulpectomy and Manual pulpectomy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteEgypt
Study dates
15 Nov 2023to 15 Jul 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 4 to 8 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • 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.

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Faculty of Dentistry, Cairo university

    Cairo, 11553

Other trials in Egypt

About this study

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

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.

Being tested
Rotary pulpectomy, Manual pulpectomy
Keywords
Rotary instrumentation, pulpectomy, primary molars, obturation quality

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Rotary pulpectomyProcedure or surgery

    Also called (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 (Fanta AF baby* rotary files and Endo Radar* rotary device).

  • Manual pulpectomyProcedure or surgery

    Also called Manual H files, Mani*)

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

Study groups in NCT06157021
Study groupRoleWhat they receive
Rotary pulpectomyExperimentalRotary pulpectomy using rotary files (Fanta AF baby* rotary files and Endo Radar* rotary device
Receives: Procedure: Rotary pulpectomy
Manual pulpectomyActive comparatorManual pulpectomy using manual H files, Mani*)
Receives: Procedure: Manual pulpectomy

What is being measured

The primary outcome is the main question the study is designed to answer.

  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)

    Measured: Immediately after the intervention

Secondary outcomes (1)
  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

    Measured: Immediately after the intervention and after 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Dec 2023
  2. Study start15 Nov 2023
  3. Primary completion15 Jun 2024
  4. Study completion15 Jul 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized controlled parallel double blinded study
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06157021
Sponsor's protocol ID
1-11-23
Acronym
RCT
Status last verified
Feb 2026
First submitted
12 Nov 2023
Last updated
11 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: No plan to share

Questions about this trial

What is this clinical trial studying?

A study testing Rotary pulpectomy and Manual pulpectomy in people with Necrotic Primary Molars, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

parental acceptance (time frame: Immediately after the intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Feb 2026.

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