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OpenTrials
Completed

NCT Number: NCT05669118

Dental Autotransplantation or Immediate Single Implant for the Replacement of a Hopeless Molar.

The aim of this comparative study is to know the differences between the soft tissue volume changes around the autotransplanted tooth and the dental implant placed immediately after the extraction of a posterior tooth. Patient-centered results will also be obtained after having received one or the other treatment.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Clínica Dental Esteve

Alicante, 03001, Spain

About this study

Dental autotransplantation has high levels of success in permanent teeth with open apex. The results of success in permanent teeth with closed apex are somewhat lower but sufficient to consider the treatment as a viable alternative and to extend the therapeutic range of the treatment to older ages.

The aim of this prospective observational investigation is to evaluate the dimensional and attachment changes that occur in the treated areas and in the autotransplanted teeth respectively of adult patients with permanent teeth with closed apex. All adult patients receiving a dental autotransplantation between the years 2022 and 2023 will be included.

Pre-treatment, volume and insertion parameters will be recorded before and one year after treatment. The comparison with the extraction and dental implant treatment will be made using the digital records that are usually obtained during the performance of this treatment. The comparison will be made with the same number of patients who have been recruited for the dental autotransplant treatment, and the volumetric changes that occur will also be analyzed.

The volume comparisons will be carried out using the Medit Link digital measurement software (Medit, Seoul, Republic of Korea) and data will be obtained and analyzed statistically in order to draw the appropriate conclusions.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Patients in ASA-I health status
  • Aged between 18 and 80 years,
  • Present a tooth in need of extraction with a mature candidate donor tooth compatible with the recipient bed
  • Acceptance of proposed treatment of dental autotransplantation

Exclusion criteria

  • Unavailability of a candidate donor tooth
  • Refusal of proposed treatment of dental autotransplantation

Treatment and study plan

Tooth Autotransplantation

Procedure

Place another tooth in the place of the newly extracted tooth in the same patient.

Other names: Dental autotransplant

Immediate implant

Procedure

Place a dental implant immediately after tooth extraction.

Other names: Type 1 implant

Primary outcomes

  1. Soft tissue volume changes

    Time frame: 2 times measurement: day 0 and 6 months after

    Soft tissue volume changes in the buccal side of the site in mm3

  2. Periodontal probing pocket depth

    Time frame: 6 months after

    Periodontal probing pocket depth in mm

Secondary outcomes

  1. Patients satisfaction after treatment

    Time frame: 6 months after the reception of the treatment

    Satisfaction assessed by Numeric Rating Scale (NRS) form 0 to 10, being 0 "not satisfied at all" and 10 "very satisfied".

Sponsors and collaborators

Lead sponsor

Aula Dental Avanzada

Other

Registry information

Official study title

Dental Autotransplantation or Immediate Single Implant for the Replacement of a Hopeless Molar: a Comparative Case Series Study.

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Dec 30, 2022
Registry last updated
Apr 26, 2024

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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