NCT07077694

Brief Summary

Aims to detect the Accuracy of Artificial Intelligence Technology in Detecting the Presence of Missed Canals of Endodontically Treated Mandibular Second Molar. Will Artificial intelligence software, CBCT and Clinical visual examination with dental operating microscope differs in the detection of presence of missed canals of endodontically treated human mandibular second molar ?

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
3

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Dec 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 25, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

July 1, 2025

Completed
21 days until next milestone

First Posted

Study publicly available on registry

July 22, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 29, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 29, 2025

Completed
Last Updated

July 22, 2025

Status Verified

October 1, 2024

Enrollment Period

10 months

First QC Date

July 1, 2025

Last Update Submit

July 11, 2025

Conditions

Keywords

Morphological variationPresence of missed canalsCBCTAIArtificial intelligenceClinical visual examinationdental operating microscopemandibular second molar

Outcome Measures

Primary Outcomes (1)

  • Presence of missed canals

    Pre Operative and At the end of the treatment within 1 week

Secondary Outcomes (1)

  • Morphological variation

    Pre Operative and At the end of the treatment within 1 week

Study Arms (2)

Presence of missed canals

ACTIVE COMPARATOR
Procedure: Root Canal Retreatment

Morphological variation

ACTIVE COMPARATOR
Procedure: Root Canal Retreatment

Interventions

if Retreatment was needed, local anesthesia using 1.8 ml (one cartridge) of 4% articaine with 1:100,000 epinephrine local anesthetic solution, administered with end -loading cartridge aspirating syringe and a 27-gauge long needle. Under rubber dam isolation, All carious tissue and existing coronal restorations were thoroughly removed using a round bur, an endodontic access cavity, canal preparation and removal of existing root canal filling, irrigation with 2.6% NAOCL and saline, determining the working length using apex locator and PA radiograph, to be 0.5 to 1 mm shorter than radiographic apex, Drying the canal with paper point and obturation to achieve a dense, well adapted Monoblock obturation. A post-obturation periapical radiograph was taken to confirm the quality of the fill in terms of length, density, then sealed by a temporary restorative material.

Also known as: Re-RCT
Morphological variationPresence of missed canals

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • \- 1) Patients must be medically free from any systemic disease that can affect root canal treatment.
  • \) Age range of the patient should be between 18 - 50 years old. 3) No sex predilection. 4) Patients must have good oral hygiene. 5) Patients with root canal-treated teeth. 6) Restorable teeth. 7) Positive patient acceptance for participating in the study. 8) Patients can sign informed consent.

You may not qualify if:

  • \- 1) Patients with very poor oral hygiene. 2) Patients above 50 years and below 18 years. 3) Pregnant women after taking detailed history and pregnancy test must be in the first visit.
  • \) Psychologically disturbed patients. 5) Tooth periodontally affected with grade 2 or 3 mobility. 6) Non restorable teeth. 7) Tooth with abnormal anatomy and calcified canals.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Oral and Dental Medicine future university

Cairo, Cairo Governorate, 11835, Egypt

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
DIAGNOSTIC
Intervention Model
SEQUENTIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
B.D.S

Study Record Dates

First Submitted

July 1, 2025

First Posted

July 22, 2025

Study Start

December 25, 2024

Primary Completion

October 29, 2025

Study Completion

October 29, 2025

Last Updated

July 22, 2025

Record last verified: 2024-10

Locations