NCT07542223

Brief Summary

Chronic apical periodontitis is a chronic inflammatory condition characterized by periapical tissue destruction and alveolar bone resorption as a result of the host response to pulpal infection, often presenting asymptomatically. The aim of this study is to comprehensively evaluate the relationship between genetic polymorphisms and periapical lesion healing in individuals with chronic apical periodontitis at clinical and radiological levels. Despite standardized root canal treatment protocols, variability in healing outcomes among individuals suggests a potential role of genetic factors in this process. This prospective observational study will include patients diagnosed with chronic apical periodontitis based on clinical and radiographic findings. All participants will undergo standardized endodontic treatment. At baseline, periapical radiography and cone-beam computed tomography (CBCT) will be performed to enable three-dimensional volumetric assessment. Follow-up evaluations will be conducted at 6 months with clinical examination and periapical radiography, and at 12 months with repeat CBCT imaging to assess volumetric changes in lesion size. All radiographic procedures will be performed in accordance with the ALARA principle, using an endodontic field of view (FOV). Prior to treatment, saliva samples will be collected for DNA isolation, and single nucleotide polymorphisms in selected cytokine gene regions will be analyzed. The primary outcome measure will be the change in periapical lesion volume over time, which will be statistically evaluated in relation to genetic profiles. This comprehensive approach is expected to enhance the understanding of healing mechanisms in apical periodontitis, improve the predictability of treatment outcomes, and contribute to the development of personalized, risk-based treatment strategies in endodontic practice.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
96

participants targeted

Target at P50-P75 for all trials

Timeline
16mo left

Started Feb 2026

Geographic Reach
1 country

1 active site

Status
active not recruiting

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 Progress17%
Feb 2026Sep 2027

Study Start

First participant enrolled

February 1, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

April 14, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 21, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Expected
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

April 21, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

April 14, 2026

Last Update Submit

April 14, 2026

Conditions

Keywords

chronic apical periodontitisCone beam computed tomographySingle nucleotide polymorphismRoot canal treatment

Outcome Measures

Primary Outcomes (1)

  • genetic analysis of participant patients

    This study is expected to contribute to a deeper understanding of the biological foundations of apical periodontitis and to support the development of personalized endodontic treatment approaches. Identifying the effects of single nucleotide polymorphisms (SNPs) related to inflammatory response and bone metabolism (IL1B, IL6, TNFA, RANKL, OPG) on periapical healing will help clarify why apical periodontitis exhibits different clinical courses among individuals.

    from enrollment to the 12 month follow-up

Interventions

Saliva samples will be used for DNA isolation utilizing the QIAamp DNA Mini Kit. DNA quality will be assessed using a NanoDrop spectrophotometer. Allele-specific SNP genotyping assays will be loaded onto the Fluidigm 96.96 Dynamic Array IFC, and genotyping data will be analyzed using the BioMark Data Collection Software by calculating FAM and HEX signal intensities.

Also known as: SNP

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients aged between 18 and 65 years who present with non-vital teeth showing negative responses to cold testing and electric pulp testing, negative responses to percussion and palpation tests, and radiographic evidence (via intraoral periapical radiography) of apical radiolucency with a Periapical Index (PAI) score of 3 or 4 in mandibular molar teeth will be included in the study.

You may qualify if:

  • Patients aged between 18 and 65 years
  • Devital mandibular molar teeth with asymptomatic apical periodontitis
  • Teeth showing negative response to percussion and palpation tests
  • Teeth with negative responses to cold test and electric pulp testing
  • Teeth with a Periapical Index (PAI) score of 3 or 4
  • Patients classified as ASA I
  • Patients without any genetic disorders (e.g., Down syndrome, congenital insensitivity to pain, etc.)

You may not qualify if:

  • Teeth with internal or external resorption
  • Teeth with a history of trauma
  • Teeth with vertical or horizontal root fractures
  • Teeth with grade 3 mobility and loss of function
  • Teeth that cannot be isolated with rubber dam or are not restorable
  • Pregnant women or patients with suspected pregnancy
  • Root canal curvature greater than 25° according to Schilder's classification
  • Patients with generalized periodontitis
  • Presence of periodontal pocket depth greater than 3 mm in the involved tooth
  • Patients classified as ASA II or higher
  • Presence of preoperative swelling, sinus tract, or pain on palpation
  • Patients with bruxism
  • Teeth with suspected periodontal-endodontic lesions
  • Teeth with a PAI index below 2 or above 5

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Atatürk Üniversitesi Diş Hekimliği Fakültesi

Erzurum, Yakutiye, Turkey (Türkiye)

Location

Biospecimen

Retention: SAMPLES WITH DNA

saliva

MeSH Terms

Interventions

Polymorphism, Single Nucleotide

Intervention Hierarchy (Ancestors)

Polymorphism, GeneticGenetic VariationGenetic Phenomena

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
12 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
prof.dr.

Study Record Dates

First Submitted

April 14, 2026

First Posted

April 21, 2026

Study Start

February 1, 2026

Primary Completion (Estimated)

August 1, 2026

Study Completion (Estimated)

September 1, 2027

Last Updated

April 21, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations