Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
NCT07237620

The Effect of Different Intracanal Medicaments on Periapical Lesion Healing

Led by Mustafa Kemal University · Updated on 2025-11-20

60

Participants Needed

1

Research Sites

80 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is planned to evaluate the effects of two different intracanal medicaments-calcium hydroxide and diclofenac sodium-on periapical healing following endodontic retreatment. Fifty-four patients will be included and randomly assigned into two groups according to the type of medicament used. All procedures will be performed by a single experienced endodontist under standardized clinical conditions. Periapical lesion healing will be assessed radiographically at baseline and after 12 months using fractal analysis to quantitatively evaluate bone regeneration. The primary outcome will be the change in the fractal dimension values between the initial and follow-up radiographs.

CONDITIONS

Official Title

The Effect of Different Intracanal Medicaments on Periapical Lesion Healing

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 60 years
  • Systemically healthy individuals classified as ASA I-II
  • Presence of apical periodontitis after primary root canal treatment
  • Single-rooted, root-filled mandibular teeth with a periapical index score of 3 or higher
  • Initial endodontic treatment performed at least four years prior or presence of clinical symptoms and signs
  • Root canal fillings with satisfactory or poor quality as defined by obturation criteria
  • Indications for retreatment including post-treatment apical periodontitis, poor obturation quality, symptoms like spontaneous pain, tenderness, or sinus tract formation
Not Eligible

You will not qualify if you...

  • History of psychiatric disorders
  • Allergic reactions
  • Pregnancy
  • Use of analgesics within seven days before treatment
  • Use of antibiotics within the previous three months
  • Teeth with periodontal pocket depth greater than 4 mm
  • Severe coronal destruction preventing rubber dam placement
  • Vertical root fracture
  • Internal or external root resorption
  • Ankylosis
  • Overfilling or open apex
  • Teeth that have undergone surgical or nonsurgical retreatment after primary therapy
  • Teeth with perforation or fractured instruments

AI-Screening

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Trial Site Locations

Total: 1 location

1

Merve Sarı

Hatay, Antakya, Turkey (Türkiye), 31060

Actively Recruiting

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Research Team

M

Merve Sarı, DDS,MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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