Immediate Dentoalveolar Restoration Compared to Bio-oss

Fresh Sockets With Buccal Resorption Clinical Trial

— IDRBio-oss  

Official title:

Immediate Dentoalveolar Restoration Compared to Demineralized Bovine Bone in Immediate Implants Placed in Fresh Sockets With Buccal Bone Resorption: 18-months Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03202030
• Other study ID #: Udelar
• Status: Completed
• Phase: N/A
• Start date: January 2016
• Est. completion date: January 2020

Study information

• Verified date: May 2022
• Source: Federal University of Rio Grande do Sul
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This randomised controlled trial compares the immediate dentoalveolar restoration and bovine demineralised bone in immediate implants placed in fresh sockets with buccal resorption. A total of 34 patients will be included and followed clinically and radiographically for 18 months. Patient centred outcomes will also be evaluated.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 34
• Est. completion date: January 2020
• Est. primary completion date: December 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Tooth extraction indicated for teeth in anterior area between second premolars

Exclusion Criteria:

• Diabetes and other systemic conditions that may affect osseointegration

Related Conditions & MeSH terms

• Fresh Sockets With Buccal Resorption

Intervention

Procedure:
• Immediate dentoalveolar restoration
Block of bone removed from the tuber and placed in the buccal resorption of the socket together with an immediate implant
• Demineralized bovine bone
Block of demineralised bovine bone placed in the buccal resorption of the socket together with an immediate implant

Locations

Country	Name	City	State
Uruguay	Universidad de La Republica del Uruguay	Montevideo

Sponsors (2)

Lead Sponsor	Collaborator
Federal University of Rio Grande do Sul	University of the Republic, Uruguay

Country where clinical trial is conducted

Uruguay, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Buccal-palatal thickness		18 months
Secondary	Oral-health related quality of life	The OHIP-14 will be applied and satisfaction will also be recorded	18 months