Validation Use of Implants and Abutments With Biologically Oriented Preparation Technique

Universidad Complutense de Madrid

Status

Completed

Conditions

Dental Implant-Abutment Design

Treatments

Procedure: Implant surgery and restoration

Study type

Interventional

Funder types

Other

Identifiers

NCT05051839

14/532

Details and patient eligibility

About

This randomized clinical trial aims to validate and to establish indications for using implants with biological oriented preparation technique (I.B.O.P.T.) for implant supported prosthetic treatment as an option looking for better stability and control of associated soft and hard tissues compared with conventional implants and conventional abutments with finishing lines preparation technique.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female ≥18 years old.
Need for implant-supported fixed prosthesis in the posterior area of the upper or lower jaw (up to 2 implants and three units bridge);
Adequate bone quality and quantity at the implant site to allow the insertion of Sweden and Martina Premium or Prama (Due Carrare, Padova, Italy), of diameters 3.8, 4.25 or 5 mm and lengths between 10 and 13 mm.
Healthy ASA type I and II patients.
Full-mouth plaque index <20.

Exclusion criteria

Smokers ≥10 cigarettes/day.
Presence of implant-supported restorations adjacent to the study site.
Active periodontitis defined as the presence of pockets with probing depth (PD) ≥5 mm and bleeding on probing (BoP).
Systemic medication that contraindicates surgery (bisphosphonates or steroid therapy).
Uncontrolled diabetes.
Severe bruxism.
Pregnancy.
Previous history of radiotherapy.