Immediate Dentoalveolar Restoration Compared to Bio-oss

NCT ID: NCT03202030

Last Updated: 2022-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-01-31

Study Completion Date

2020-01-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Fresh Sockets With Buccal Resorption

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

IDR

Immediate dentoalveolar restoration conducted with bone removed from the tuber

Group Type EXPERIMENTAL

Immediate dentoalveolar restoration

Intervention Type PROCEDURE

Block of bone removed from the tuber and placed in the buccal resorption of the socket together with an immediate implant

Bio-oss

Bovine demineralized bone (Bio-oss Collagen) applied on the buccal resorption of the immediate implant

Group Type ACTIVE_COMPARATOR

Demineralized bovine bone

Intervention Type PROCEDURE

Block of demineralised bovine bone placed in the buccal resorption of the socket together with an immediate implant

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Immediate dentoalveolar restoration

Block of bone removed from the tuber and placed in the buccal resorption of the socket together with an immediate implant

Intervention Type PROCEDURE

Demineralized bovine bone

Block of demineralised bovine bone placed in the buccal resorption of the socket together with an immediate implant

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

IDR

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

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

Exclusion Criteria

* Diabetes and other systemic conditions that may affect osseointegration
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of the Republic, Uruguay

OTHER

Sponsor Role collaborator

Federal University of Rio Grande do Sul

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Alex Nogueira Haas

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Universidad de La Republica del Uruguay

Montevideo, , Uruguay

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Uruguay

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Udelar

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.