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NCT Number: NCT07314580

Clinical and Radiological Evaluation of Dental Autotransplantation in the Anterior Region in Young Patients

This study aims to evaluate the clinical, radiographic, functional, and patient-reported outcomes of premolar autotransplantation used to replace anterior maxillary teeth in young patients. The study has an ambispective observational design, including a retrospective cohort (patients treated between December 2019 and December 2025) and a prospective cohort (patients enrolled until December 2028).

Participants aged 7 to 15 years who received or will receive premolar autotransplantation to replace an anterior tooth will be followed clinically and radiographically for up to 5 years. Outcomes include tooth survival, periodontal and pulpal healing, root development, complications, orthodontic interactions, restorative needs, and patient satisfaction. The study seeks to identify prognostic factors and long-term success indicators for dental autotransplantation in growing patients.

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Key information

Age range

7 year–15 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Dental Esthetic BCN

Barcelona, Barcelons, 08034, Spain

Location status: Recruiting

Location contact

Xavier Rodriguez Ciurana, PhD

CONTACT

[email protected]

+34 936404390

About this study

Premolar autotransplantation is a biologically favorable treatment option for young patients who have lost an anterior maxillary tooth due to trauma, resorption, or restorative failure. This study evaluates outcomes of autotransplantation combining a retrospective cohort (patients treated from 2019 to 2025) and a prospective cohort (patients recruited until 2028). All procedures follow a standardized clinical protocol including digital planning with CBCT and STL models, 3D-printed donor tooth replicas, guided socket preparation when needed, atraumatic donor extraction, extraoral time under 5 minutes, and semirigid splinting.

Clinical and radiographic follow-ups occur at 1 week, 15 days, 1, 2, 3, 6, 9, and 12 months, and annually up to 5 years. Evaluations include mobility, sensitivity, percussion sound, periodontal measurements, gingival recession, root development (Moorrees stages), pulpal healing, and radiographic signs of complications such as resorption or ankylosis. Digital analysis of soft and hard tissues and esthetic outcomes is performed with STL models and CBCT when indicated.

The study also assesses the influence of orthodontic variables (previous treatment, appliance type, timing of movement after transplantation) and restorative parameters (reconstruction chronology). Patient-reported outcomes include satisfaction, esthetics, function, and oral health-related quality of life using validated questionnaires.

Data from both cohorts are anonymized and analyzed descriptively and comparatively, with multivariable modeling to identify prognostic factors.

Although enrollment is defined at the participant level, outcome measures are assessed at the level of the autotransplanted tooth. Participants may contribute more than one autotransplanted tooth to the analysis.

The study will provide long-term evidence regarding success, survival, complications, and perceived outcomes of premolar autotransplantation in growing patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 7 to 15 years.
  • ASA I classification.
  • Loss or indication for extraction of a maxillary anterior tooth (teeth 12, 11, 21, or 22) due to trauma, resorption, or restorative reasons.
  • Availability of a donor first or second premolar with root development between one-half and complete root length.
  • Ability to complete at least 2 years of follow-up.
  • Parent/guardian consent and minor assent obtained for prospective cases.

Exclusion criteria

  • Patients older than 15 years.
  • Severe systemic disease.
  • Inability or unwillingness to attend scheduled follow-up visits.
  • Lack of a suitable donor premolar.

Treatment and study plan

premolar autotransplantation

Procedure

Premolar autotransplantation performed using a standardized clinical protocol including digital planning (CBCT and STL models), 3D-printed donor tooth replicas, guided or conventional socket preparation, atraumatic donor extraction, extraoral time under 5 minutes and semirigid splinting. Clinical and radiographic follow-up is performed up to 5 years.

Other names: Tooth Autotransplantation, Dental Autotransplantation

Primary outcomes

  1. Number of Autotransplanted Teeth with Clinical and Radiographic Success

    Time frame: Up to 5 years

    Number of autotransplanted teeth that fulfill all predefined success criteria at each follow-up visit:

    Absence of ankylosis Absence of progressive root resorption Physiological mobility Normal percussion sound Functional stability Absence of clinical signs of infection Each autotransplanted tooth is considered an independent observational unit. In participants with more than one autotransplanted tooth, each tooth is evaluated separately.

Secondary outcomes

  1. Survival Rate of the Autotransplanted Tooth

    Time frame: Up to 5 years

    Number of autotransplanted teeth remaining in situ without extraction during follow-up.

  2. Root Development Stage of the Autotransplanted Tooth

    Time frame: Up to 5 years

    Root development stage of the autotransplanted tooth assessed radiographically using the Moorrees classification.

  3. Pulpal Healing Status of the Autotransplanted Tooth

    Time frame: Up to 5 years

    Number of autotransplanted teeth presenting pulpal healing, defined as pulp canal obliteration or maintained pulp vitality without signs of necrosis, based on clinical testing and radiographic findings.

  4. Periodontal Probing Depth of the Autotransplanted Tooth

    Time frame: Up to 5 years

    Mean periodontal probing depth (in millimeters) measured at six sites around the autotransplanted tooth.

  5. Gingival Recession of the Autotransplanted Tooth

    Time frame: Up to 5 years

    Gingival recession measured in millimeters from the cemento-enamel junction to the gingival margin at the mid-buccal site of the autotransplanted tooth.

  6. Incidence of Root Resorption

    Time frame: Up to 5 years

    Number of autotransplanted teeth presenting inflammatory or replacement root resorption detected radiographically.

  7. Incidence of Ankylosis

    Time frame: Up to 5 years

    Number of autotransplanted teeth presenting clinical and/or radiographic signs of ankylosis.

  8. Orthodontic Treatment After Autotransplantation

    Time frame: Up to 5 years

    Time (in months) from autotransplantation to initiation of orthodontic tooth movement of the autotransplanted tooth.

  9. Number of Restorative Procedures Performed on the Autotransplanted Tooth

    Time frame: Up to 5 years

    Total number of restorative procedures performed on each autotransplanted tooth during follow-up.

  10. Oral Health-Related Quality of Life (OHIP-14 Score)

    Time frame: Up to 5 years

    Mean score of the Oral Health Impact Profile-14 (OHIP-14) questionnaire. Score range: 0-56. Higher scores indicate worse oral health-related quality of life.

  11. Patient Satisfaction with Esthetic Outcome

    Time frame: Up to 5 years

    Patient-reported satisfaction with dental esthetics measured using a Visual Analog Scale (VAS) from 0 to 10, where higher scores indicate greater satisfaction.

Other outcomes

  1. Change in Alveolar Bone Volume at the Autotransplantation Site

    Time frame: Up to 5 years

    Change in alveolar bone volume (in cubic millimeters, mm³) at the autotransplantation site assessed by CBCT superimposition at baseline and follow-up visits, when imaging is clinically indicated.

  2. Change in Gingival Tissue Volume at the Autotransplantation Site

    Time frame: Up to 5 years

    Change in gingival tissue volume (in cubic millimeters, mm³) assessed by STL model superimposition at baseline and follow-up visits, when digital models are available.

Study contacts

Contact information is provided by the study sponsor or research team.

Jordi Cadellans, DDS

CONTACT

[email protected]

+34 934011235

Montserrat Mercadé, PhD

CONTACT

[email protected]

+34 934011235

Sponsors and collaborators

Lead sponsor

University of Barcelona

Other

Registry information

Official study title

Clinical, Radiographic, Functional and Psychosocial Evaluation of Premolar Autotransplantation to the Anterior Maxillary Region in Young Patients: An Ambispective Observational Study

Acronym: YATA

Important dates

Study start
2019
Primary completion
2029
Study completion
2029
First posted
Jan 2, 2026
Registry last updated
Jan 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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