Replanting severely damaged single-rooted teeth to try to save them and restore bone

Assessment of Treatment Outcomes and Alveolar Bone Changes Following Intentional Replantation of Hopeless Periodontally Involved Single-Rooted Teeth - A Pre-test, Post-test Interventional Study

Not applicable Interventional University of Fujairah · NCT06893107

This project will try intentional replantation to save single-rooted teeth judged hopeless because of chronic periodontitis in adults aged 18–70.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment45 (estimated)
Ages18 Years to 70 Years
SexAll
SponsorUniversity of Fujairah Academic / other
Locations1 site (Fujairah, Emirate of Fujairah)
Trial IDNCT06893107 on ClinicalTrials.gov

What this trial studies

This is a single-arm before-and-after interventional study where adults with single-rooted teeth considered hopeless from periodontic lesions undergo intentional replantation. Teeth are atraumatically extracted, handled extraorally for less than 15 minutes with possible root-end treatment, and replanted and splinted, followed by standard postoperative care. Outcomes include radiographic bone and periodontal tissue changes measured with CBCT at baseline and 9 months, clinical signs such as pain, swelling, and mobility, and patient-reported satisfaction and quality of life. Data collection combines clinical exams and imaging to compare status before and after the procedure.

Who should consider this trial

Good fit: Adults 18–70 with a single-rooted tooth judged hopeless from true periodontic lesions who have ≥50% radiographic bone loss, probing depth ≥5 mm, Grade III mobility of the targeted tooth, ASA class 1–2, and who prefer replantation and can attend follow-up visits.

Not a fit: Patients with vertical root fractures, prior failed intentional replantation, severe anatomic limitations, multi-rooted teeth, poor systemic health, or unwillingness to adhere to follow-up are unlikely to receive benefit from this procedure.

Why it matters

Potential benefit: If successful, this approach could allow some patients to keep teeth that would otherwise be extracted, improve local bone support and symptoms, and enhance oral-related quality of life.

How similar studies have performed: Previous case series and small cohort reports of intentional replantation have shown mixed but sometimes promising outcomes, but large randomized trials are lacking.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

Patients meeting the specified criteria will be included in the study.

* The patients with American Society of Anesthesiologists physical status classification 1 and 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 (minimal to slight increased mobility without functional impairment) of adjacent teeth.
* Distance between the targeted tooth and adjacent teeth less than 2 millimetres.
* Patient preference for tooth retention through intentional replantation over extraction.

Exclusion Criteria:

* Previous history of failed IR.
* Severe anatomical limitations in the treatment area.
* Unwillingness to adhere to follow-up protocols

Where this trial is running

Fujairah, Emirate of Fujairah

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Chronic PeriodontitisChronic periodontitisPeriodontally compromised toothIntentional replantation
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.