The Role of a New Prosthodontics Device in Hard and Soft Tissue Changes After Subcrestal Implant Placement (NABUT)

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

Status: Completed

Conditions: Edentulous Alveolar Ridge

Treatments: Device: Healing Abutment; Procedure: Crestal Implant; Device: Gingival Former Abutment; Procedure: Subcrestal Implant; Device: Prosthetic Crown

Study type: Interventional

Funder types: Other

Identifiers

NCT06182670

NABUT NP 4078

Details and patient eligibility

About

The present randomized controlled trial aims to assess the influence of a new prosthodontics device (Gingival Former Abutment -GFA) on peri-implant bone loss and soft tissue changes and health after subcrestal oral implant placement.

The participants will be divided in two groups and receive either crestal implant placement and traditional healing abutment or subcrestal implant placement and GFA.

Clinical and radiographic examination will be performed at implant placement surgery, prosthetic load, 6 and 12 months follow-up.

Full description

According to current literature, physiological bone loss around oral implants is expected after placement and load (1 mm during the first year and 0.2 mm each subsequent year). Different implant designs and surgical protocols have been tested to minimize bone resorption, and subcrestal implant placement partially seems to overcome this issue. However, if this procedure increases the length of the transmucosal tunnel, increasing the risk of peri-implant soft tissue infection.

The GFA was created to limit both the loss of peri-implant crestal bone and the extension of the transmucosal tunnel. The GFA follows the "one abutment one time" concept, which is believed to limit disturbances of the peri-implant hard and soft tissues healing due to the removal of the traditional healing abutments during prosthetic load procedures. Our objective is to validate or deny this claim.

The study is a monocentric, pragmatic, single-blinded, randomized clinical trial (RCT) of parallel design. The trial will have a one-year duration, with data collection at the surgical phase, at implant load and 6 and 12 months after load. The primary outcome will be radiographical MBL (marginal bone level) changes around the implant. Secondary outcomes will be the assessment of the peri-implant soft tissues.

Enrollment: 40 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Ability to comprehend and sign informed consent.

• Male and female subjects, aged 18-75 years, inclusive.

• Good general health (free of systemic diseases such as diabetes, HIV infection or genetic disorder, ongoing malignant disease of any type that could influence the outcome of the treatment and might interfere with the evaluation of the study objectives).

• Good oral health (no decay, periapical or periodontal lesions, PI and BOP <25%).

• Patient with posterior single missing tooth:

  • for at least 5 months,
  • mandibular or maxillary,
  • intercalated (distance between teeth more than 7.5 mm),
  • at least 11 mm of height residual bone (from bone crest to maxillary sinus or inferior alveolar nerve),
  • at least 5 mm of bone width (buccal - palatal/lingual).

• Availability for the 12-month duration of the study.

Exclusion criteria

• Not willing to follow the agreed protocol.
• Presence of orthodontic appliances.
• Smokers more than 10 cigarettes per day.
• Chronic obstructive pulmonary disease and asthma.
• Tumors or significant pathology of the soft or hard tissues of the oral cavity.
• Current radiotherapy or chemotherapy.
• Pregnant or lactating women.
• Parafunctions like bruxism.
• Previous interventions to increase bone thickness in the implant area.
• Current or past assumption of medications that may influence surgical therapy and/or interfere with healing following surgical treatment.
• Systemic diseases that constitute a contraindication to surgical therapy and/or interfere with healing following surgical treatment.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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40 participants in 2 patient groups

Subcrestal implant and gingival former abutment (GFA)

Experimental group

Description:

The subjects receive a subcrestal implant and a prosthodontic device (GFA) immediately during the surgery. The GFA will not be removed upon prosthetic load. It will be an integral part of the prosthetic finalization.

Treatment:

Device: Gingival Former Abutment

Procedure: Subcrestal Implant

Device: Prosthetic Crown

Crestal implant and traditional abutment

Active Comparator group

Description:

The subjects receive a crestal implant and healing abutment. The healing abutment will be replaced by a definitive abutment to the prosthetic load.

Treatment:

Procedure: Crestal Implant

Device: Healing Abutment

Device: Prosthetic Crown