Simplified vs Conventional Drilling Protocol for Implant Placment

NCT ID: NCT06780956

Last Updated: 2025-01-17

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

PHASE3

Total Enrollment

46 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-01

Study Completion Date

2024-03-01

Brief Summary

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Despite the growing interest in these alternative drilling protocols, there is a lack of robust clinical evidence evaluating their long-term effects on MBL. The aim of the present study was therefore, to evaluate the effect of implant site preparation technique (conventional drilling versus simplfied) on change in the marginal bone level and insertion torque.

Detailed Description

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Conditions

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MBL Bone Loss

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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conventional

Conventional Drilling Protocol

Group Type ACTIVE_COMPARATOR

Conventional

Intervention Type OTHER

conventional drilling protocol using full sequence

simplfied

simplfied drilling protocol

Group Type EXPERIMENTAL

simplfied

Intervention Type OTHER

3 burrs for implant placment

Interventions

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Conventional

conventional drilling protocol using full sequence

Intervention Type OTHER

simplfied

3 burrs for implant placment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients without any systemic pathologies that could be considered grounds for absolute contraindication.
* Adult patients who agreed to participate in the study and signed the informed consent form.
* Patients who smoked fewer than ten cigarettes per day.
* Patients who were not completely edentulous.
* Patients who were partially edentulous in the posterior maxillary or mandibular area and did not require the use of regenerative techniques.
* Patients with an area of healed, mature bone at least three months post-extraction.

Exclusion Criteria

* Patients missing teeth in the esthetic zones 13-23 and 33-43 (second and fifth sextants).
* Patients who smoked more than ten cigarettes per day.
* Patients with a bleeding index greater than 30%.
* Patients with dental caries or periodontal disease.
* Pregnant or lactating women.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universidad Católica San Antonio de Murcia

OTHER

Sponsor Role lead

Responsible Party

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Artiom Lijnev

MSc

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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UCAM

Murcia, , Spain

Site Status

Countries

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Spain

Other Identifiers

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CE092002

Identifier Type: -

Identifier Source: org_study_id

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