Extra-short vs. Non-extra-short Dental Implants Splinted on the Same Prosthesis
NCT ID: NCT04927819
Last Updated: 2025-04-17
Study Results
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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RECRUITING
102 participants
OBSERVATIONAL
2021-05-11
2025-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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short-length implant (<6.5 mm)
BTI Implant
BTI Dental implants are non-active medical device, single use, non resterilizable, biocompatible and sterile devices made of alloplastic materials (Titanium) intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g. bridge, single-tooth, overdenture).
non-short length implant (≥6.5 mm)
BTI Implant
BTI Dental implants are non-active medical device, single use, non resterilizable, biocompatible and sterile devices made of alloplastic materials (Titanium) intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g. bridge, single-tooth, overdenture).
Interventions
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BTI Implant
BTI Dental implants are non-active medical device, single use, non resterilizable, biocompatible and sterile devices made of alloplastic materials (Titanium) intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g. bridge, single-tooth, overdenture).
Eligibility Criteria
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Inclusion Criteria
* Have planned a fixed multiple prosthesis supported by implants \<6.5 mm in length and implants ≥ 6.5 mm in length within 15 days before the inclusion of the patient in the study.
* Planning of supported prostheses from 2 to 4 implants dental
* Have a previously performed CBCT (Cone Beam Computed Tomography)
* Availability to be observed during the period of tracing
* Signature of the informed consent
Exclusion Criteria
* Complete prostheses
* Unitary prostheses
18 Years
ALL
No
Sponsors
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Fundación Eduardo Anitua
OTHER
Responsible Party
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Principal Investigators
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Eduardo Anitua, MD
Role: PRINCIPAL_INVESTIGATOR
Clinica Eduardo Anitua
Locations
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Clinica Eduardo Anitua
Vitoria-Gasteiz, , Spain
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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FIBEA_02_EP/20/Extracortos
Identifier Type: -
Identifier Source: org_study_id
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