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Antimicrobial Effect of Calcium Silicate and Pectin as Intracanal Medications in Necrotic Teeth With Periapical Lesions

Antimicrobial Effect of Calcium Silicate and Pectin as Intracanal Medications in Necrotic Teeth With Periapical Lesions :A Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07423663
Enrollment
63
Registered
2026-02-20
Start date
2024-09-01
Completion date
2026-04-01
Last updated
2026-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asymptomatic Apical Periodontitis

Keywords

Asymptomatic Apical Periodontitis, pectin, bio-c temp, Calcium Hydroxide

Brief summary

It is tackling antimicrobial resistance in endodontics, specifically comparing different intracanal medications used in root canal treatment. Given the growing concern over resistant bacterial strains, our study aims to evaluate the effectiveness of various medicaments in eliminating endodontic pathogens while minimising the risk of resistance development. By integrating microbiological analysis and clinical relevance, our research seeks to provide evidence-based recommendations for optimising intracanal disinfection protocols and improving treatment outcomes in endodontic infections.

Interventions

Patients receiving CaOH (Metapaste) intracanal medication

DRUGCalcium silicate based intracanal medication

Patients receiving Calcium silicate based (Bio-C Temp) intracanal medication

DRUGPectin

Patients receiving Pectin intracanal medication

Sponsors

Suez Canal University
Lead SponsorOTHER
University of Leeds
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients presenting with a single rooted mandibular premolar tooth with a closed apex and a single patent canal type I in Vertucci's classification (Vertucci et al., 1974). * Having a necrotic pulp. * A pocket depth measurement of \< 3 mm. * Teeth with no previous history of endodontic treatment. * Teeth with periapical lesions of endodontic origin having a periapical index score of 4 or 5 (Orstavik et al., 1986) * Patients who took antibiotics within the period of three months before the study. * Non-restorable teeth. * Teeth with periodontal pockets deeper than 4mm, with or without concomitant or combined endo-perio communication * Multirooted teeth. * Previously initiated or treated teeth. * Teeth with root canal calcifications or resorption. * Teeth with internal/external root resorption or root fracture. * Immune-compromised patients or patients with systemic diseases i.e. (diabetes mellitus, human immunodeficiency virus, leukemia, neutropenia, undergoing chemo- or systemic corticosteroid therapy) * Teeth with root curvature of more than 15 degrees. * Pregnant women * Patients with known sensitivity to the medicaments used in this study.

Design outcomes

Primary

MeasureTime frameDescription
Microbiome ChangesFrom enrollment to the end of treatment at 2 weeksCompare the changes in the microbial composition of the biofilm inside the infected root canal before and after chemo-mechanical preparation and before and after intracanal medicaments application using DNA next-generation sequencing.

Countries

Egypt

Contacts

PRINCIPAL_INVESTIGATOROmar Montaser, M.D.Sc

Suez Canal University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026