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Randomized Clinical Trial to Evaluate the Predictability of 5.5 mm Dental Implants

F

Fundación Eduardo Anitua

Status

Completed

Conditions

Partial-edentulism

Treatments

Device: BTI Implant

Study type

Interventional

Funder types

Other

Identifiers

NCT04929743
BTI_02_EC/20/4.5

Details and patient eligibility

About

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.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

15 participants in 2 patient groups

5.5 mm implants
Experimental group
Treatment:
Device: BTI Implant
>6.5 mm implants
Active Comparator group
Treatment:
Device: BTI Implant

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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