Insertion Protocol of Convergent Transmucosal Design Implants

University of Cagliari

Status: Enrolling

Conditions: Implant Site Reaction

Treatments: Procedure: Sub-crestal Implant placement; Procedure: Equi-crestal Implant placement

Study type: Interventional

Funder types: Other

Identifiers

NCT06254885

PramaNAV

Details and patient eligibility

About

The aim of this randomized clinical study is the evaluation of the peri-implant mucosal tissues and the marginal bone level, after positioning the transition shoulder from the intraosseous to the transmucosal portion, with an equicrestal position (at the level of the bone crest) or subcrestal (under the bone crest level).

Full description

The primary outcomes will be the measurement of the marginal bone level (MBL) at various time intervals and the evaluation of the soft tissues according to a score defined as Pink Esthetic Score (PES). Secondary outcomes will be plaque index (PI); the bleeding index (BI), biological complications (peri-implant mucositis, peri-implantitis, abscesses), implant failure, prosthetic complications (chipping, fractures) and prosthetic failure.

The subjects recruited for the study will be those belonging to the oral surgery department of the San Giovanni di Dio Hospital in Cagliari.

Each patient will receive only one implant or, in any case, only one implant per patient will be included in the analysis. A random sequence will be generated via Randomization.com, useful for assigning patients into the equicrestal and subcrestal implant placement groups.

All patients will undergo the same preoperative, intraoperative and postoperative procedures.

Preoperative procedures An intraoral radiograph of the edentulous site will be performed. Upper and lower alginate impressions will be made on each patient for planning and fabrication of surgical guides, all patients will receive rigorous oral hygiene and instructions will be provided to improve and maintain home oral hygiene.

Intraoperative procedures After local anesthesia of the site to be operated on, a full thickness mucoperiosteal flap will be elevated, after lifting the flap the implant site will be prepared according to the manufacturer's protocol. Before implant placement, the sealed envelope will be opened for random assignment of the patient to one of the two groups. The implant will therefore be positioned, depending on the assignment group, in an equicrestal or subcrestal position, in the latter case a further step with the last preparation drill will be performed to deepen the site.

The flap will be sutured after placement of the healing screw and specific hygiene instructions for the healing site will be given to the patient. The appropriate analgesic and antibiotic therapy will be prescribed.

An intraoral x-ray will be performed in a standardized and repeatable manner to assess bone levels.

The patient will be followed following the following follow-up scheme, reserving the right to recall the patients involved even at longer time intervals to evaluate the aforementioned outcomes also in the medium (24 months) and long (5-10 years) term.

1. week: healing check
2. weeks: healing check and suture removal

1 month: healing check 3 months: prosthesis and intraoral x-ray, measurement of soft tissue parameters via PES after positioning of the prosthetic crown 6 months: intraoral x-ray and PES 12 months: intraoral x-ray and PES The marginal bone level will be measured using ImageJ software (NIH freeware) on the distal and mesial aspects of each implant at each time point where it is foreseen.

Enrollment: 25 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age >18 years
• Absence of periodontal disease
• Full mouth plaque score and full mouth bleeding score less than or equal to 25%
• Sufficient bone height and width to place an implant in a prosthetically guided position without performing bone grafting procedures
• Stable occlusion

Exclusion criteria

• Smokers (more than 10 cigarettes a day)
• Medical conditions that contraindicate implant surgery
• Pregnant and breastfeeding patients
• Patients with a history of therapy with bisphosphonates or biologics
• Patients undergoing chemotherapy or radiation therapy of the head and neck
• Decompensated diabetes
• Severe bruxism
• Poor oral hygiene or uncooperative patients (incomplete data collection or failure to attend scheduled check-up appointments)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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25 participants in 2 patient groups

Sub-crestal

Experimental group

Description:

Implants will be placed 1mm under the bone crest level

Treatment:

Procedure: Sub-crestal Implant placement

Equi-crestal

Active Comparator group

Description:

Implants will be placed at the bone crest level

Treatment:

Procedure: Equi-crestal Implant placement