ISQ Differences Between Different Implants in Post-extraction Sockets

NCT ID: NCT06711744

Last Updated: 2025-03-28

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

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-31

Study Completion Date

2027-02-28

Brief Summary

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Two different implants will be used in post-extraction sockets and ISQ will be recorded monthly from insertion moment to 12 months of follow up to understand if ISQ can be affected by implant macro design

Detailed Description

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Conditions

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Bone Healing Implant Stability

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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TISSUE LEVEL X

Implants with aggressive macro design

Group Type ACTIVE_COMPARATOR

Implant stability quotient

Intervention Type DIAGNOSTIC_TEST

Screw a smart peg into the implant and record the values from a dedicated device

TISSUE LEVEL C

Implants with less aggressive macro design

Group Type EXPERIMENTAL

Implant stability quotient

Intervention Type DIAGNOSTIC_TEST

Screw a smart peg into the implant and record the values from a dedicated device

Interventions

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Implant stability quotient

Screw a smart peg into the implant and record the values from a dedicated device

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patients (at least 18 years old) presenting with failing tooth.
* no recession of gingival contour of tooth to be extracted
* no periodontal bone loss of neighboring teeth
* no implants in neighboring teeth
* class I extraction socket (intact buccal wall)
* atraumatic extraction of the tooth with intact socket walls remaining.

Exclusion Criteria

* deep bite (severe II class)
* systemic disease (diabetes, osteoporosis)
* heavy smokers (more than 10 cigarettes/day)
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Rome Tor Vergata

OTHER

Sponsor Role lead

Responsible Party

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Paolo Carosi

Post-doctoral Researcher

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Paolo Carosi

Rome, RM, Italy

Site Status RECRUITING

Countries

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Italy

Central Contacts

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Paolo Carosi, PhD

Role: CONTACT

+393277998699

Facility Contacts

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Paolo Carosi, PhD

Role: primary

3277998699

Other Identifiers

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TLCVSTLX

Identifier Type: -

Identifier Source: org_study_id

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