None listed
Conditions
Brief summary
Objectives: To evaluate the clinical outcomes, peri-implant parameters, microbial environment and success rates of three different placement times of single wide implants for replacing molar teeth. Materials and mehtods: Wide –diameter implants will be placed at different times following extraction of a single molar tooth in either mandibular or maxillary arches. A total of 39 participants will be randomly allocated to three equal sized groups (13 per group), a control and one of the test groups as follows: Control group: Implants placed after complete bone healing Test group 1: Implants immediately place after extraction Test group II: Implants placed after an early osseous healing time (3-5 weeks).
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
(1) Require a single molar tooth extraction in either jaw. (2) Aged 18 or over. (3) Physical status P1 or P2, according to the classification system of the American Society of Anesthesiologists (ASA) (4) Controlled oral hygiene. (5) Type I-III bone quality (Lekholm and Zarb, 1985). (6) Presence of 3-4 remaining osseous walls. (7) Good compliance and commitment to attend follow-up review appointments. (8) Willing to provide informed consent.
Exclusion criteria
(1) Traumatic tooth extraction. (2) Dehiscence in extraction socket wall greater than 4 mm. (3) Inadequate bone quality (Type IV) (Lekholm and Zarb, 1985). (4) Localized infection (suppuration at the surgical field) (5) Ankylosed teeth. (6) Aggressive or refractory periodontitis. (7)Severe bruxism or parafunctional habits. (8) Large occlusal discrepancies. (9) Medical risk patients.