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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04929743
Other study ID # BTI_02_EC/20/4.5
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 11, 2021
Est. completion date July 31, 2023

Study information

Verified date July 2022
Source Fundación Eduardo Anitua
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main aim of this clinical trial is to analyze the survival rate of short-length implants (<4.5 mm) in partial edentulism subjects. 6.5 mm length implants will be used as control arm. Additionally, others clinical parameters (marginal bone loss and prosthetic associated complications) will be measured.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 15
Est. completion date July 31, 2023
Est. primary completion date July 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years - Clinical indication to place a prosthetic bridge supported by a maximum of 4 implants in the posterior sectors - Bone height in the area of interest sufficient to place implants 6.5mm length dental implants - Availability to be observed during the follow-up period - Signature of the informed consent Exclusion Criteria: - Need to perform bone augmentation surgery prior to implant placement surgery - Smokers (> 10 cigarettes per day) - Patients with poorly controlled diabetes - Patients on chronic treatment with non-steroidal anti-inflammatory drugs - Patients receiving oral or intravenous bisphosphonates - Patients under chemotherapy or radiotherapy treatment - Patients receiving systemic corticosteroids

Study Design


Related Conditions & MeSH terms


Intervention

Device:
BTI Implant
Placement of dental implants of 5.5 vs >6.5 mm length

Locations

Country Name City State
Spain Clinica Eduardo Anitua Vitoria

Sponsors (1)

Lead Sponsor Collaborator
Fundación Eduardo Anitua

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival of implants Survival of implants at one year post-implantation 1 year
Secondary Marginal bone loss Marginal bone loss at one year post-implantation 1 year
Secondary Incidence of bleeding on probing 1 year
Secondary Incidence of prosthetic or implant complications 1 year
Secondary Probing pocket depth 1 year
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