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Not yet recruitingNCT07351682Updated Jan 20, 2026

Antibacterial Activity of Calcium Hydroxide and Betamethasone in Apical Periodontitis

An observational study in Apical Periodontitis, sponsored by Duygu Degirmencioglu. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-01-20.

Sponsored by Duygu Degirmencioglu · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
45
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Apical periodontitis is a chronic inflammatory disease caused by bacterial infection of the root canal system. Although mechanical cleaning and shaping reduce most microorganisms, bacteria may persist in areas that are difficult to reach, making the use of intracanal medicaments between treatment sessions clinically important.

Calcium hydroxide is one of the most commonly used intracanal medicaments because of its antibacterial properties. However, some resistant microorganisms, such as Enterococcus faecalis, may survive when calcium hydroxide is used alone. Therefore, combining calcium hydroxide with other agents, such as iodoform or corticosteroids, may improve its antibacterial effectiveness.

The purpose of this study is to compare the antibacterial activity of calcium hydroxide used alone or in combination with iodoform (Metapex) or betamethasone in patients with apical periodontitis. Bacterial load in root canals will be evaluated using droplet digital PCR (ddPCR), a highly sensitive molecular method that allows absolute quantification of bacteria. The results of this study are expected to provide evidence to support optimal intracanal medicament selection in endodontic retreatment cases.

Read the detailed description

Apical periodontitis is a chronic inflammatory condition of periapical tissues that develops as a result of persistent bacterial infection within the root canal system. While chemomechanical preparation significantly reduces the microbial load, bacteria may remain in anatomical complexities such as dentinal tubules, isthmuses, and apical ramifications. For this reason, intracanal medicaments are widely used between treatment sessions to enhance disinfection and improve treatment outcomes.

Calcium hydroxide is the most frequently used intracanal medicament due to its high pH and antibacterial properties. Nevertheless, certain microorganisms, particularly Enterococcus faecalis, have been shown to survive in alkaline environments, limiting the effectiveness of calcium hydroxide when used alone. To overcome this limitation, calcium hydroxide has been combined with various agents, including iodoform and corticosteroids, with the aim of enhancing antibacterial activity and reducing periapical inflammation.

Droplet digital PCR (ddPCR) is a novel molecular technique that enables absolute quantification of bacterial DNA without the need for standard curves and is less affected by PCR inhibitors compared to conventional quantitative PCR methods. Despite its advantages, the use of ddPCR in clinical endodontic research remains limited, particularly in in vivo studies evaluating intracanal medicaments.

This prospective, single-center clinical study aims to compare the antibacterial efficacy of three intracanal medicament protocols in patients with apical periodontitis undergoing endodontic retreatment: (1) calcium hydroxide alone, (2) calcium hydroxide combined with iodoform (Metapex), and (3) calcium hydroxide combined with betamethasone. Root canal samples will be collected at different treatment stages, and total bacterial load as well as Enterococcus faecalis levels will be quantified using ddPCR.

The findings of this study are expected to provide high-quality clinical evidence regarding the antibacterial effectiveness of commonly used intracanal medicaments and their combinations. The results may contribute to evidence-based decision-making in the selection of intracanal medicaments for the management of apical periodontitis, particularly in retreatment cases.

02

Conditions studied

  • Apical Periodontitis

Keywords

  • Betamethasone
  • Calcium Hydroxide
  • Enterococcus faecalis
  • Droplet Digital PCR
  • Retreatment
03

In context

Periapical Periodontitis

245 studies on the registry are indexed under Periapical Periodontitis; 64 are open to participants now.

This study's planned enrollment of 45 is below the median of 72 across 33 observational studies indexed under Periapical Periodontitis.

Browse Periapical Periodontitis studies →

Lead sponsor

This is the only study on the registry with Duygu Degirmencioglu as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of adult patients diagnosed with apical periodontitis who require endodontic retreatment and are treated at a single academic dental center.

Inclusion criteria

  • - Adults aged 18 to 65 years.
  • Patients diagnosed with apical periodontitis requiring endodontic retreatment.
  • Presence of a single tooth with radiographic evidence of apical periodontitis.
  • Ability to provide written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Use of systemic antibiotics within the previous 3 months.
  • Presence of systemic diseases that may affect healing or immune response.
  • Pregnancy or lactation.
  • Known allergy or hypersensitivity to any of the intracanal medicaments used.
  • Teeth with acute abscess, severe periodontal disease, or root fractures.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
45 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Calcium Hydroxide

    This cohort includes patients with apical periodontitis undergoing endodontic retreatment who receive calcium hydroxide as an intracanal medicament as part of routine clinical care. The selection of the intracanal medicament is based on standard clinical decision-making and is not assigned by the study protocol.

  • Calcium Hydroxide + Iodoform (Metapex)

    This cohort includes patients with apical periodontitis undergoing endodontic retreatment who receive a combination of calcium hydroxide and iodoform (Metapex) as an intracanal medicament as part of routine clinical care. The intracanal medicament is selected according to standard clinical practice and is not assigned by the study protocol.

  • Calcium Hydroxide + Betamethasone

    This cohort includes patients with apical periodontitis undergoing endodontic retreatment who receive a combination of calcium hydroxide and betamethasone as an intracanal medicament as part of routine clinical care. The choice of intracanal medicament is determined by routine clinical decision-making and is not assigned by the study protocol.

06

What researchers measure

Primary outcomes

  1. Change in Total Bacterial Load in Root Canal Samples

    The primary outcome is the change in total bacterial load in root canal samples collected during endodontic retreatment. Bacterial load will be quantified using droplet digital PCR (ddPCR) by measuring absolute bacterial DNA copy numbers at different treatment stages.

    Time frame: From baseline to 7 days after intracanal medicament application

Secondary outcomes

  1. Change in Enterococcus faecalis Levels

    This secondary outcome assesses the change in Enterococcus faecalis levels in root canal samples collected during endodontic retreatment. Enterococcus faecalis DNA will be quantified using droplet digital PCR (ddPCR) by measuring absolute DNA copy numbers before and after intracanal medicament application.

    Time frame: From baseline to 7 days after intracanal medicament application

07

Study locations

1 site
  • Istanbul Medipol University Faculty of Dentistry
    Istanbul, Istanbul 34810, Turkey (Türkiye)
    • Istanbul Medipol University Faculty of Dentistry Clinical Research Office · Contact · duygu.degirmencioglu@medipol.edu.tr · +90 212 444 85 44
    • Duygu Degirmencioglu · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07351682
Lead sponsor
Duygu Degirmencioglu
Responsible party
Duygu Degirmencioglu (Duygu Degirmencioglu, Medipol University) — Sponsor-investigator
First posted
Jan 20, 2026
Start date
Mar 1, 2026 (estimated)
Primary completion
Nov 1, 2026 (estimated)
Completion
Mar 1, 2027 (estimated)
Last update
Jan 20, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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