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Clinical Trials/NCT04933409
NCT04933409
Unknown
Not Applicable

3D Printed Donor Tooth Replica in Autotransplantation of Teeth. A Randomized Clinical Trial.

College of Medical Sciences Teaching Hospital. Nepal0 sites50 target enrollmentOctober 1, 2021
ConditionsDecayed Teeth

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Decayed Teeth
Sponsor
College of Medical Sciences Teaching Hospital. Nepal
Enrollment
50
Primary Endpoint
Operative time
Last Updated
4 years ago

Overview

Brief Summary

3D printed replicas of the donor tooth can reduce extraoral time during the autotransplantation of teeth, which can reduce dehydration and manipulation of periodontal tissue of the donor tooth, thus possibly increasing the success rate.

Detailed Description

This technique of autotransplantation has been innovated using 3-dimensional (3D) imaging and rapid prototyping.The use of a 3D-printed replica of the donor tooth is thought to minimize the risk of iatrogenic damage to the actual donor tooth. Nevertheless, no large prospective and comparative studies are available to assess the outcomes using these 3D techniques. Therefore, this study aimed to compare 3D printed replicas in autotransplantation of teeth, compared to the conventional technique. The present study will evaluate the feasibility, clinical satisfied accuracy, and stability of a novel approach for computer-aided autotransplantation of teeth. This new approach facilitated the surgical procedure and might be a viable and predictable method for autotransplantation of teeth. Application of printed 3D replicas of transplanted teeth facilitates surgical preparation of the recipient site, shortens the extra-alveolar time, and reduces the minimum the number of attempts of the donor tooth insertion at the prepared socket. Their use can significantly decrease the risk of damage to the root surface of a transplant, thus increasing the chance of success.

Registry
clinicaltrials.gov
Start Date
October 1, 2021
End Date
March 1, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
College of Medical Sciences Teaching Hospital. Nepal
Responsible Party
Principal Investigator
Principal Investigator

Ashutosh Kumar Singh

Assistant Professor

College of Medical Sciences Teaching Hospital. Nepal

Eligibility Criteria

Inclusion Criteria

  • patient presenting with decayed first molars
  • autotransplantation of third molar at the recipient site

Exclusion Criteria

  • Diabetic, pregnant patients
  • other autotransplantations (other than first molar recipient and third molar donor)

Outcomes

Primary Outcomes

Operative time

Time Frame: 1 day

Operative time from the start of socket preparation at the recipient site

Rate of Ankylosis (replacement resorption)

Time Frame: 6 months

Ankylosis (replacement resorption)

Rate of root resorption

Time Frame: 6 months

infection related root resorption

Number of teeth that fail

Time Frame: two weeks

reduced mobility (less than grade II) after 2 weeks of autotransplantation

Secondary Outcomes

  • Cost difference of the treatment(1 day)

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