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Tooth Autotransplantation and Bone Dimension Changes

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03927937
Recruitment Status : Recruiting
First Posted : April 25, 2019
Last Update Posted : April 25, 2019
Information provided by (Responsible Party):
Francisco Javier Rodriguez Lozano, Universidad de Murcia

Brief Summary:

Tooth autotransplantation is a treatment option to replace tooth with imposible prognosis. In several cases the receipt site has a reduced bone dimension. This situation may be imposible the treatment with dental implants without bone reconstruction. Autotransplantation seem to improve the anatomic characteristic of the receipt site without any reconstruction approach.

The aim of this study is to evaluate the bone dimension changes followed autotransplantation treatment.

Condition or disease Intervention/treatment Phase
Bone Loss, Alveolar Tooth Loss Bone Atrophy, Alveolar Procedure: AUTOTRANSPLANTATION TOOTH Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 20 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Tooth Autotransplantation and Bone Dimension Changes. Randomized Clinical Trial.
Actual Study Start Date : December 5, 2018
Estimated Primary Completion Date : December 30, 2019
Estimated Study Completion Date : June 30, 2020

Arm Intervention/treatment
Tooth with imposible prognosis is replace with a healthy tooth from the same patient.

Primary Outcome Measures :
  1. Change in alveolar bone 12 months after tooth autotransplantation [ Time Frame: 1 year ]
    CT-scan evaluation before surgery and 1 year after, measuring the difference in millimeters

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Tooth with imposible prognosis
  • Plaque index score less than 30%
  • No relevant systemic disease
  • Smokers (Less than 20 cigars/day)

Exclusion Criteria:

  • Pregnancy-Lactation
  • Relevant systemic disease

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03927937

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Contact: Miguel Ramón P Pecci Lloret, DDS 630492610

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Universidad de Murcia Recruiting
Murcia, Spain, 30003
Contact: Miguel Ramón PECCI LLORET    630492610   
Sponsors and Collaborators
Universidad de Murcia
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Responsible Party: Francisco Javier Rodriguez Lozano, PhD, Universidad de Murcia Identifier: NCT03927937    
Other Study ID Numbers: 2015/2018
First Posted: April 25, 2019    Key Record Dates
Last Update Posted: April 25, 2019
Last Verified: April 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Alveolar Bone Loss
Tooth Loss
Pathological Conditions, Anatomical
Periodontal Diseases
Mouth Diseases
Stomatognathic Diseases
Tooth Diseases
Bone Resorption
Bone Diseases
Musculoskeletal Diseases
Periodontal Atrophy