Narrow-diameter Implants Replacing Maxillary Lateral Incisors

NCT ID: NCT06500923

Last Updated: 2024-07-15

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

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-08-01

Study Completion Date

2024-06-15

Brief Summary

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To present the 5-year clinical, radiographic, and aesthetic outcomes in patients with congenitally missing lateral incisors (MLIs) rehabilitated with two narrow-diameter implants (NDIs).

Detailed Description

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Conditions

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Dental Implant Failed

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Ø2.9mm (Test)

Test patients have received a 2.9 Ø dental implant

Oral rehabilitation by means of implant-supported single unit crowns

Intervention Type OTHER

Surgery: Implant placement; Prothetic rehabilitation: single unit crown

Ø3.3mm (Control)

Control patients have received a 3.3 Ø dental implant

Oral rehabilitation by means of implant-supported single unit crowns

Intervention Type OTHER

Surgery: Implant placement; Prothetic rehabilitation: single unit crown

Interventions

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Oral rehabilitation by means of implant-supported single unit crowns

Surgery: Implant placement; Prothetic rehabilitation: single unit crown

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients affected by congenital missing with uni- or bilateral maxillary lateral incisors (i.e. 12 and/or 22)
* Patients with systemic health or controlled medical conditions
* Patients arrested skeletal growth as documented by two body height measurements at least one year apart not indicating continuous growth (Jensen, 2019)
* Written Informed Consent

Exclusion Criteria

* Patients contraindications to implant therapy (Hwang \& Wang, 2006, 2007) including
* Heavy smoking: \>20 cigarettes/day
* Poor oral hygiene
* Compromised compliance
* Periodontally compromised conditions
* Patients with MLI's with the canine situated in the MLI region
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Copenhagen University Hospital, Denmark

OTHER

Sponsor Role collaborator

University of Bern

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Simon Storgaard Jensen, Prof.

Role: STUDY_CHAIR

Copenhagen University Hospital, Copenhagen, Denmark

Locations

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University Hospital Copenhagen

Copenhagen, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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2012-58-0004

Identifier Type: -

Identifier Source: org_study_id

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