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Buccal and Palatal Bone Thickness and Marginal Bone Changes Implants (IBPTHPIBC)

I

International Piezosurgery Academy

Status

Completed

Conditions

Bone Implant; Complications

Treatments

Procedure: implant insertion

Study type

Observational

Funder types

Other

Identifiers

NCT05632172
maxillary contraction

Details and patient eligibility

About

The primary outcome of the study was the vertical variation of peri-implant buccal and palatal bone level from implant placement (T0) to uncovering stage (3 months later - T1)

Full description

despite various recommendations, there is insufficient evidence to set a threshold for minimal buccal bone thickness necessary to ensure peri-implant marginal bone stability and optimal aesthetic outcomes.

Therefore, the aim of the present multi-centre prospective study was to investigate the influence of buccal and palatal bone thickness at the time of implant placement on peri-implant bone remodeling during the submerged healing period, with a strict control of possible confounding factors.

Enrollment

90 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age > 18 years;
  • no smokers;
  • no history of periodontal disease;
  • healed bone crest (at least six months after tooth extraction);
  • crestal bone height ≥8 mm;
  • crestal bone with a minimum bucco-palatal width of 6 mm with no concomitant or previous bone augmentation procedures.

Exclusion criteria

  • absolute contraindications to implant surgery
  • immunological or genetic disorders;
  • uncontrolled diabetes (HBA1c > 7.5%);
  • present or past treatment with anti resorptive drugs;
  • oncologic patients;
  • history of head or neck radiotherapy;
  • alcohol or drugs abuse;
  • final insertion torque > 50 Ncm.

Trial design

90 participants in 1 patient group

maxillary group
Description:
implant insertion
Treatment:
Procedure: implant insertion

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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