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.
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.
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.
- Intra \& extra oral examination was made with aid of mirror and probe to assess the clinical inclusion criteria.
- Preoperative photographs were taken
- Preoperative radiograph were examined
Intervention:
Patients were assigned into two groups; Group A (Experimental group) (using rotary files)
- Pre-operative radiograph showing all roots and their apices.
- Local anaesthetic (to enable use of rubber dam clamp).
- Rubber dam isolation.
- Removal of caries.
- Removal of roof of pulp chamber.
- Identify root canals.
- Irrigate with concentrated sodium hypochlorite followed by normal saline (0.9%)
- Estimate working lengths of root canals keeping 2 mm short of the radiographic apex.
- Insert rotary files into canals and debride the canals lightly and gently.
- Irrigate the root canals.
- Dry canals with pre-measured paper points, keeping 2 mm from root apices.
- Canals were dried with paper points, obturated by injecting Metapex. (Meta Biomed - Metapex Root Canal Filling Material)
- 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.
- Conditions
- Necrotic Primary Molars
- 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 group | Role | What they receive |
|---|---|---|
| Rotary pulpectomy | Experimental | Rotary pulpectomy using rotary files (Fanta AF baby* rotary files and Endo Radar* rotary device Receives: Procedure: Rotary pulpectomy |
| Manual pulpectomy | Active comparator | Manual 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.
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)
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.
- First posted5 Dec 2023
- Study start15 Nov 2023
- Primary completion15 Jun 2024
- Study completion15 Jul 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Necrotic Primary MolarsStudies of the same condition, open and under way.
- More trials run by Cairo UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Cairo University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Rasha Adel Ragab, Cairo University
- Investigators
- Rasha A Ragab, Lecturer, Principal investigator, Faculty of Dentistry, Cairo University, Egypt.
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
Study at a glance
From the registry record, last updated by the sponsor on 11 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Obturation Quality in Necrotic Primary Molars After Manual Versus Rotary Pulpectomy; a Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT06157021
- Acronym / sponsor ID
- RCT / 1-11-23
- Conditions
- Necrotic Primary Molars
- Keywords
- Rotary instrumentation, pulpectomy, primary molars, obturation quality
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 40 participants (actual)
- Lead sponsor
- Cairo UniversityUniversity, hospital or other
- Study start
- 15 Nov 2023 (actual)
- Primary completion
- 15 Jun 2024 (actual)
- Study completion
- 15 Jul 2024 (actual)
- First posted
- 5 Dec 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
- Intra \& extra oral examination was made with aid of mirror and probe to assess the clinical inclusion criteria.
- Preoperative photographs were taken
- Preoperative radiograph were examined
Intervention:
Patients were assigned into two groups; Group A (Experimental group) (using rotary files)
- Pre-operative radiograph showing all roots and their apices.
- Local anaesthetic (to enable use of rubber dam clamp).
- Rubber dam isolation.
- Removal of caries.
- Removal of roof of pulp chamber.
- Identify root canals.
- Irrigate with concentrated sodium hypochlorite followed by normal saline (0.9%)
- Estimate working lengths of root canals keeping 2 mm short of the radiographic apex.
- Insert rotary files into canals and debride the canals lightly and gently.
- Irrigate the root canals.
- Dry canals with pre-measured paper points, keeping 2 mm from root apices.
- Canals were dried with paper points, obturated by injecting Metapex. (Meta Biomed - Metapex Root Canal Filling Material)
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Randomized controlled parallel double blinded study
| Arm | Type | Receives |
|---|---|---|
| Rotary pulpectomy | Experimental | Procedure: Rotary pulpectomyRotary pulpectomy using rotary files (Fanta AF baby* rotary files and Endo Radar* rotary device |
| Manual pulpectomy | Active comparator | Procedure: Manual pulpectomyManual pulpectomy using manual H files, Mani*) |
Who may qualify
- Ages
- 4 to 8 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (5 listed)
- 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.
Key exclusion criteria (7 listed)
- 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,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Rotary pulpectomyAlso: (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). | Procedure or surgery | Rotary pulpectomy |
| Manual pulpectomyAlso: Manual H files, Mani*)Pulpectomy procedures by making cleaning and shaping of root canals of necrotic primary molars using Manual H files, Mani*) | Procedure or surgery | Manual pulpectomy |
Primary outcome
parental acceptance
Time frame: Immediately after the intervention
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)
1 secondary outcome
obturation quality
Time frame: Immediately after the intervention and after 6 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Feb 2026.
- Individual participant dataSharing planned: No. No plan to share
Related trials for Necrotic Primary Molars
Active, not recruitingObservational study
Lesion Sterilization Tissue Repair and Conventional Pulpectomy in Primary Molars
Pulpitis - Irreversible, Pulp Necroses
Enrolling by invitation
Evaluation of Different Medicaments in the Management of Necrotic Primary Molars by Lesion Sterilization and Tissue Repair
Pain, Postoperative, Root Resorption
Not yet recruiting
Clinical and Radiographic Success of Calcium Hydroxide-Iodoform Paste Versus Modified Triple Antibiotic Paste for Necrotic Primary Molars in Children
Dental Pulp Necrosis, Periapical Diseases
Not yet recruitingEarly Phase 1
Chloramphenicol, Tetracycline, Zinc Oxide and Eugenol Paste (CTZ Paste) for Emergency Dental Treatment in Public Health Settings: A Randomized Trial
Pulp Disease, Dental, Pulp Necrosis
Not yet recruitingPhase 1/2
Lesion Sterilization and Tissue Repair Antibiotic Paste Versus Zinc Oxide and Eugenol Pulpectomy for Treatment of Primary Molars With Pulp Necrosis
Pulp Necrosis
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Rasha A Ragab, Lecturer principal investigator
Faculty of Dentistry, Cairo University, Egypt.
1 site in 1 country: see every site and its status.
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.