Bioactive Surfaces vs. Conventional Surfaces in Implants Placed in Atrophic Maxilla With Simultaneous Sinus Lift

Sponsor
Studio Odontoiatrico Associato Dr. P. Cicchese e L. Canullo (Other)
Overall Status
Recruiting
CT.gov ID
NCT05500911
Collaborator
(none)
40
1
2
21.4
1.9

Study Details

Study Description

Brief Summary

In this controlled clinical study, a maxillary sinus lift (crestal approach) with OSSIX® Bone will be performed, and then implants MultiNeO CS (control group) and NINA MultiNeO NH (test group) will be inserted in edentulous posterior maxillae of study subjects. .+the clinical and radiographic results of the rehabilitation of posterior edentulous maxillary areas, obtained with traditional surface implants (MultiNeO CS, control group), are compared with those obtained with bioactive surface implants (NINA - MultiNeO NH, test group ).

Condition or Disease Intervention/Treatment Phase
  • Procedure: sinus lift
  • Procedure: implant placement
N/A

Detailed Description

In this post- market controlled clinical study, the tested CE-marked dental implants are MultiNeO CS 1930 and NINA MultiNeO NH 9330, both manufactured by Alpha-Bio Tec. NeO or MultiNeO is defined as a system since it includes three types of connections: a conical narrow connection (CHC), a conical standard conical connection (CS) and an Internal Hex connection (IH). The fixture has a straight coronal part, a slightly tapered body, and a conical apical part. We will use MultiNeO CS to treat control group. One of the MultiNeO CS biggest clinical advantages since it is as good at bone type 4 as it is at bone type 1, 2 or 3.

MultiNeO CS has an implant surface with a sub-micron scale roughness created by Aluminum oxide blasting and double acid etching.

NINA MultiNeO NH is used for tret group, it has got an innovative bioactive surface.

NINA MultiNeO NH surface is a combination of the abovementioned roughening process and the creation of titanium oxide nano structure. Its hydrophilic part is created by resorbable salt thus maintaining its hydrophilicity Patient requiring sinus floor elevation with native bone crest height > 4 mm will be enrolled.Although a variety of implant surface are available for implant supported rehabilitation, the first hypothesis is that NINA MultiNeO NH Alpha-Bio Tec will be present faster osteointegration time compared to MultiNeO CS when adopted to rehabilitate of missing teeth in case of critical areas such as in the posterior mandible with critical bone defects. The second hypothesis is that NINA MultiNeO NH will promote a better apical bone regeneration in patients treated with sinus lift compared to MultiNeO CS due to its bioactive surface.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
After the sinus lift procedure (performed with OSSIX® BONE on all study subjects), control group will be treated with a traditional implant surface (MultiNeO CS), test group will be treated with a bioactive surfaced implant (NINA MultiNeO NH)After the sinus lift procedure (performed with OSSIX® BONE on all study subjects), control group will be treated with a traditional implant surface (MultiNeO CS), test group will be treated with a bioactive surfaced implant (NINA MultiNeO NH)
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluation of a Bioactive Surface in Posterior Maxillary Sites: Controlled Clinical Trial
Actual Study Start Date :
Apr 22, 2022
Anticipated Primary Completion Date :
Feb 1, 2024
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: NINA- MultiNeO NH

After the sinus lift procedure (performed with OSSIX® BONE on all study subjects) treatment group will be treated with a bioactive surfaced implant (NINA MultiNeO NH)

Procedure: sinus lift
when residual bone height is >4 mm sinus lift through crestal approach procedure will be performed and after sinus flor elevation, OSSIX® Bone will be placed in the sinus cavity.
Other Names:
  • sinus floor elevation
  • Procedure: implant placement
    Implant will be placed in edentulous area

    Active Comparator: MultiNeO CS

    After the sinus lift procedure (performed with OSSIX® BONE on all study subjects) control group will be treated with a traditional implant surface (MultiNeO CS)

    Procedure: sinus lift
    when residual bone height is >4 mm sinus lift through crestal approach procedure will be performed and after sinus flor elevation, OSSIX® Bone will be placed in the sinus cavity.
    Other Names:
  • sinus floor elevation
  • Procedure: implant placement
    Implant will be placed in edentulous area

    Outcome Measures

    Primary Outcome Measures

    1. Marginal bone loss [6 months after implant placement]

      radiographic evaluation of the marginal bone level around the implant using a periapical x ray. marginal bone loss is in millimeters and indicates how many millimeters of bone has been lost

    2. Marginal bone loss [12 months after implant placement]

      radiographic evaluation of the marginal bone level around the implant using a periapical x ray. marginal bone loss is in millimeters and indicates how many millimeters of bone has been lost

    3. Implant stability [immediately after implant placement]

      check implant stability using resonant frequency analysis (RFA) Resonance frequency analysis (RFA) provides objective measurements of implant stability in a non-invasive way on the bone-implant interface. The results of the resonance frequency analysis are transformed into implant stability quotient (ISQ) values. ISQ, implant stability quotient, depends on the transducer used and is recorded as a number between 1 and 100, 100 representing the highest degree of stability. Transducers are designed for specific implant types and calibrated by the manufacturer.

    4. Implant stability [2 months after implant placement]

      Resonance frequency analysis (RFA) provides objective measurements of implant stability in a non-invasive way on the bone-implant interface. The results of the resonance frequency analysis are transformed into implant stability quotient (ISQ) values. ISQ, implant stability quotient, depends on the transducer used and is recorded as a number between 1 and 100, 100 representing the highest degree of stability. Transducers are designed for specific implant types and calibrated by the manufacturer.

    5. Implant stability [4 months after implant placement]

      Resonance frequency analysis (RFA) provides objective measurements of implant stability in a non-invasive way on the bone-implant interface. The results of the resonance frequency analysis are transformed into implant stability quotient (ISQ) values. ISQ, implant stability quotient, depends on the transducer used and is recorded as a number between 1 and 100, 100 representing the highest degree of stability. Transducers are designed for specific implant types and calibrated by the manufacturer.

    6. insertion torque curve [During implant placement (T0 baseline]

      The Insertion torque data were recorded and exported as a curve The torque curve records the amount of energy that was needed for arrive at the positioning of the implant. unit of measurement of torque is Newton centimeter (Ncm)

    Secondary Outcome Measures

    1. Apical Bone regeneration [6 months after implant placement]

      Apical bone regeneration is calculated by the difference in volume between CBCT at baseline and 6 months follow-up

    2. Evaluation the effects of bioactive implant surface (NINA- MultiNeO NH) in Apical Bone regeneration performed under the schneiderian membrane lining the maxillary sinus. Apical Bone regeneration defines the osseoinductive potential of a surface. [12 months after implant placement]

      Apical bone regeneration is calculated by the difference in volume between CBCT at baseline and 6 months follow-up

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • edentulous posterior maxillae

    • residual bone height > 4mm

    • healthy periodontal conditions

    Exclusion Criteria:
    • smokers over 5 cigarettes/day

    • Pregnancy (confirmed by verbal inquiry)

    • Chronic systemic pathologies and neoplastic of the Oro-Facial District

    • bisphosphonates intake

    • Any sites where an implant already failed sites

    • Untreated Periodontitis

    • Sites with acute infections

    • Chronic inflammatory diseases of the oral cavity

    • Autoimmune diseases (cortisone intake)

    • Allergy declared to one or more medicaments to be used during treatment

    • Alcoholics patients and/or drug addicts

    • collagen hypersensitivity.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Studio Odont.Associato Dr.P.Cicchese E L.Canullo Rome Italy/Rome Italy 00198

    Sponsors and Collaborators

    • Studio Odontoiatrico Associato Dr. P. Cicchese e L. Canullo

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Luigi Canullo, Principal investigator, Studio Odontoiatrico Associato Dr. P. Cicchese e L. Canullo
    ClinicalTrials.gov Identifier:
    NCT05500911
    Other Study ID Numbers:
    • ABT2
    First Posted:
    Aug 15, 2022
    Last Update Posted:
    Aug 15, 2022
    Last Verified:
    Aug 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Luigi Canullo, Principal investigator, Studio Odontoiatrico Associato Dr. P. Cicchese e L. Canullo
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 15, 2022