Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
Healthy Volunteers
NCT06893107

Study on Treatment Results and Bone Changes After Replanting Severely Affected Teeth - A Before-and-After Study.

Led by University of Fujairah · Updated on 2025-11-26

45

Participants Needed

1

Research Sites

102 weeks

Total Duration

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AI-Summary

What this Trial Is About

This research aims to evaluate the effectiveness of intentional replantation (IR) as a treatment for single-rooted teeth diagnosed as hopeless due to true periodontic lesions. The study will assess changes in alveolar bone and periodontal tissues, symptom resolution, and patient-reported outcomes (satisfaction and quality of life) following the procedure. Cone beam computed tomography (CBCT) imaging will be used to track radiographic changes at baseline and 9 months, while clinical examinations will monitor symptom resolution, including pain, swelling, and tooth mobility. The study is a single-arm pre-test, post-test interventional design conducted at the College of Dentistry, University of Science and Technology Fujairah (new name: University of Fujairah). Participants will include adults aged 18-70 with single-rooted teeth deemed hopeless due to periodontic lesions. Participants will undergo intentional replantation, and data will be collected through clinical examinations, radiographic images, and patient questionnaires at baseline and 9 months. Statistical analysis will compare pre- and post-treatment outcomes using paired-samples t-tests or Wilcoxon signed-rank tests, depending on data normality. The study aims to provide a comprehensive evaluation of intentional replantation, contributing valuable insights into its clinical effectiveness for managing complex dental conditions.

CONDITIONS

Official Title

Study on Treatment Results and Bone Changes After Replanting Severely Affected Teeth - A Before-and-After Study.

Who Can Participate

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with American Society of Anesthesiologists physical status classification 1 or 2
  • Radiographic bone loss of at least 50% around the targeted tooth
  • Probing depth of at least 5 millimetres around the targeted tooth
  • Grade III mobility (extreme mobility) of the targeted tooth according to Miller's classification
  • Grade II mobility or less of adjacent teeth
  • Distance between targeted and adjacent teeth less than 2 millimetres
  • Patient prefers intentional replantation to extraction for tooth retention
Not Eligible

You will not qualify if you...

  • Previous history of failed intentional replantation
  • Severe anatomical limitations in the treatment area
  • Unwillingness to follow study follow-up protocols

AI-Screening

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Trial Site Locations

Total: 1 location

1

Dental Clinic, College of Dentistry, University of Fujairah,

Fujairah, Emirate of Fujairah, United Arab Emirates, 2202

Actively Recruiting

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Research Team

N

Nabeel Ayappali Kalluvalappil, MDS

CONTACT

T

Tamer Hamed Hassan, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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