Case Selection and Treatment Protocol for Immediate Dental Implants in the Esthetic Zone
Jaw, Edentulous, Partially, Acquired Absence of Single Tooth
About this trial
This is an interventional treatment trial for Jaw, Edentulous, Partially focused on measuring Dental implants, Esthetic score, Immediate implants, Gingival biotype
Eligibility Criteria
Inclusion Criteria:
- The patient is 18 years or older.
- Ability to understand and provide informed consent before starting the study.
- Ability and willingness to comply with all study requirements.
- The patient, if of child-bearing potential, has a negative urine pregnancy test.
- Adequate oral hygiene to allow for implant therapy consistent with standards of care.
- Adequate bone volume to accommodate the planned endosseous dental implant placement according to immediate placement protocols utilizing Straumann Bone Level implants RC (Regular Crossfit) 4.1mm or Bone Level Implant NC (Narrow Crossfit) 3.3 mm at 8, 10,12 or 14mm in length.
- One tooth in the anterior maxilla (first pre-molar to first pre-molar) requiring extraction resulting in a single- tooth gap planned to be restored with a dental implant as determined by the patient's dental provider.
- The site to be treated is surrounded by two natural teeth.
- Except the site to be treated, none of the maxillary incisors, canines and first pre-molars display marginal soft tissue recession.
- Following extraction, intact extraction socket bony walls are present.
- Primary stability of implant consistent with standards of care is achieved at the time of implant placement.
- Patient must be able to pay for fees related to the surgical implant placement related to extraction, grafting of the implant site, and half of the cost of the crown at the time of implant placement.
Exclusion Criteria:
- Patient reports tobacco use within the last five years. Tobacco use for this study is defined as a current smoking habit with moderate or heavy smoking (more than 10 cigarettes per day) or tobacco chewing use.
- History of alcoholism or drug abuse within the past 5 years.
- Severe wear with an etiology of bruxism or clenching habits.
- Patient has significant untreated periodontal disease (grade III or IV), caries, or clinical or radiographic signs of infection within two adjacent tooth positions of implant area.
- History of HIV infection, Hepatitis B or C.
- Patients with a history of systemic disease that precludes standard dental implant therapy or alters daily activities to a level consistent with ASA (American Society of Anesthesiologists) III classification (including cardiovascular, hepatic, renal, gastrointestinal, metabolic, neurologic, pulmonary, endocrine, autoimmune, or psychiatric disorders).
- Presence of local inflammation or mucosal diseases such as lichen planus.
- Patient history consistent with high risk for subacute bacterial endocarditis.
- Current hematological disorder or warfarin (or similar) therapy.
- Patient has a disease that affects bone metabolism, such as, but not limited to, osteoporosis, hyperthyroidism, hyperparathyroidism, congenital connective tissue disorders (e.g., osteogenesis imperfecta), or Paget's disease.
- Patient is taking medications or having treatments known to have an effect on bone turnover, including: thiazide diuretics, calcitonin, systemic steroids, bisphosphonates, vitamin D (>800 IU/day), estrogen or progesterone therapy.
- Current steroid treatment: defined as any person who within the last two years has received for two weeks a dose equivalent to 20 mg hydrocortisone.
- Patient currently undergoing chemotherapy.
- Patient history of radiation treatment to the head or neck.
- Physical or mental handicaps that would interfere with patient's ability to exercise good oral hygiene on a regular basis.
- Use of any investigational drug or device within the 30 day period immediately prior to implant surgery.
- Patient is pregnant.
- Extraction sites having anatomic conditions that preclude immediate implant placement.
Sites / Locations
- Graduate Periodontics, Dental School, UTHSCSA
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Type 1 implant and thin biotype
Type 1 implant and thick biotype
In this group, immediate implant placement (SLActive implant) is performed in patients with thin tissue biotype. In addition to implant placement bone grafting of the void between the implant and the fresh extraction socket, bone grafting the buccal aspect of the buccal plate (overcontouring) and soft tissue grafting (connective tissue) are performed.
In this group, immediate implant placement (SLActive implant) is performed including bone grafting of the void between the implant and the fresh extraction socket.