A Prospective Clinical and Radiographic Assessment on New Platform-switched Laser Lok Implants

Tel Aviv Sourasky Medical Center

Status

Unknown

Conditions

Preserve Crestal Bone Level and Gingival Margin Around Dental Implants

Treatments

Device: platform-switch tapered internal implants

Study type

Interventional

Funder types

Other

Identifiers

TASMC 13 AS 177-13-TLV CTIL

Details and patient eligibility

About

To investigate the hard and soft tissue adaptation and maintenance to the Laser-Lok® microchannels permanent abutment/ new Laser-Lok® implant assembly by performing clinical and radiographic evaluations.
To investigate the effect of inter-implant spacing (minimum of 2 or 3 mm) on hard and soft tissues.
To perform clinical and radiographic evaluations on these abutment/implant assemblies up to 2 years.

Full description

Screening (Inclusion/ Exclusion Criteria)
Day of Surgery: Dental CT scan/ periapical radiograph / clinical picture / clinical examination (probing depth, BOP, gingival recession).
Implant Restoration Day: Post-restoration periapical radiograph/ clinical picture/ clinical examination (probing depth, BOP, gingival recession).
6 month, 1 Year and 2 Year Post Restoration: periapical radiograph / clinical picture / clinical examination (probing depth, BOP, gingival recession).

Enrollment

10 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:1. Male or female, between 20-70 years of age, who request dental implant treatment options for rehabilitation.

Subjects who are willing to sign an informed consent, participate and return for follow-up visits.
Subjects without significant medical history and currently not on medications that might complicate the results.
Subjects presenting with an edentulous area requiring a tooth-replacement option.

Exclusion Criteria:1. Subjects who do not meet all the inclusion criteria or who will not cooperate with the protocol schedule.

Subjects who received and failed a previously placed dental implant. 3. Subjects who require an onlay ridge augmentation procedure in the area to achieve adequate bone volume for the placement of dental implants.
Subjects who have significant untreated periodontal disease, caries, infection or chronic inflammation in the oral cavity within two adjacent tooth positions of the clinical trial area.
Subjects who have used nicotine-containing products within 3 weeks prior to surgery.
Subjects who are insulin-dependent diabetic or if their Hgb1c levels > 6.5%. 7. Subjects who have had a history of malignancy within the past 5 years (except for basal or squamous cell carcinoma of the skin or in situ cervical carcinoma).
Subjects who are nursing or pregnant. 9. Subjects who are presently taking medications (except estrogen/progesterone therapy) or those who are undergoing treatment that in known to have an effect on bone turnover.
Subjects who have diseases that affect bone metabolism (excluding idiopathic osteoporosis).
Subjects with a history of an autoimmune disease, documented allergy or multiple allergies to any component of the agents used in this study.
Acutely infected defect site. 13. Immediate implant site.