Randomized Clinical Trial to Evaluate the Predictability of 5.5 mm Dental Implants

NCT ID: NCT04929743

Last Updated: 2025-02-25

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-11

Study Completion Date

2024-11-27

Brief Summary

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The main aim of this clinical trial is to analyze the survival rate of short-length implants (\<4.5 mm) in partial edentulism subjects. 6.5 mm length implants will be used as control arm. Additionally, others clinical parameters (marginal bone loss and prosthetic associated complications) will be measured.

Detailed Description

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Conditions

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Partial-edentulism

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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5.5 mm implants

Group Type EXPERIMENTAL

BTI Implant

Intervention Type DEVICE

Placement of dental implants of 5.5 vs \>6.5 mm length

>6.5 mm implants

Group Type ACTIVE_COMPARATOR

BTI Implant

Intervention Type DEVICE

Placement of dental implants of 5.5 vs \>6.5 mm length

Interventions

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BTI Implant

Placement of dental implants of 5.5 vs \>6.5 mm length

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Age ≥ 18 years
* Clinical indication to place a prosthetic bridge supported by a maximum of 4 implants in the posterior sectors
* Bone height in the area of interest sufficient to place implants 6.5mm length dental implants
* Availability to be observed during the follow-up period
* Signature of the informed consent

Exclusion Criteria

* Need to perform bone augmentation surgery prior to implant placement surgery
* Smokers (\> 10 cigarettes per day)
* Patients with poorly controlled diabetes
* Patients on chronic treatment with non-steroidal anti-inflammatory drugs
* Patients receiving oral or intravenous bisphosphonates
* Patients under chemotherapy or radiotherapy treatment
* Patients receiving systemic corticosteroids
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fundación Eduardo Anitua

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Clinica Eduardo Anitua

Vitoria-Gasteiz, , Spain

Site Status

Countries

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Spain

Other Identifiers

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BTI_02_EC/20/4.5

Identifier Type: -

Identifier Source: org_study_id

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