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Autotransplantation of dental pulp from third molars into teeth with endodontic needs

Autogenous Transplantation of dental pulp from third molars into teeth with Irreversible Pulpitis and Pulp Necrosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-23khtjk
Enrollment
Unknown
Registered
2021-09-03
Start date
2021-06-25
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental pulp necrosis

Interventions

Experimental group: 14 individuals (men or women) over 18 years old, with need for third molar extraction and endodontic needs (pulp necrosis or irreversible pulpitis). Extraction of the third molar w
and 2nd surgical procedure for extraction of the third molar and consecutive pulp transplantation in the recipient tooth and provisional sealing. The parameters observed will be bone lesion regression

Sponsors

Universidade Federal do Rio Grande do Norte
Lead Sponsor
Departamento de odontologia
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who need endodontic treatment; presence of formed third molars; receptor teeth uniradicular

Exclusion criteria

Exclusion criteria: Patients under 18 years old; third molars with complicated extractions or that require dental section; little remnant of healthy teeth or that need the placement of intraradicular pins

Design outcomes

Primary

MeasureTime frame
Efficient pulp transplantation, with responsive pulp and pulp/dentin regeneration, verified through radiographic tests evaluating the regression of periapical lesions; the absence or presence of dental pain; and pulp sensitivity test to cold and heat. Data collected 2 weeks before the intervention and 32 weeks after the intervention. From the finding of regression in the lesion in millimeters, evaluated by comparing pre and postoperative radiographic exams, being classified as: Absent, stable, reduced or increased. Use of a numerical pain scale in the pre- and postoperative periods, ranging from 1 to 10; and finding a positive response to the pulp sensitivity test in the postoperative period.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactFabio Dametto
dametto71@hotmail.com+55 (84) 98871-4246

Outcome results

None listed

Source: REBEC (via WHO ICTRP)