Clinical Evaluation of Vertical Inter-implant Papilla Height in Platform Matched Implants in Comparison to Morse Connection Abutments

• Study is to be conducted in the Oral Medicine and Periodontology department, Faculty of Oral and Dental Medicine - Cairo University, Egypt.
• Patients are to be selected from the outpatient clinic of the department of Oral Medicine and Periodontology-Cairo University.

Intervention:

Clinical examination:

• Evaluation of the patient's general condition of the oral cavity, to make sure it complies with the criteria required to be enrolled in the study in terms of oral hygiene, pathological conditions, occlusion and inter-arch space.
• Evaluation of the periapical condition and crestal bone level using a periapical radiograph.
• Evaluation of the soft tissue biotype by trans-gingival piercing using a periodontal probe.
• Width of keratinized gingiva (measured by a periodontal probe from the gingival margin to the mucogingival junction). It is measured at three areas (mesial, midbuccal and distal).

SURGICAL PROTOCOL (T0):

• Patients meeting the inclusion criteria, CBCT analysis and extensive diagnosis is done to plan for treatment.
• After randomization patients are assigned to one of the two groups
• After profound anesthesia administration, a full thickness crestal flap is reflected, sequential osteotomy of the implant sites to the desired depth is performed with great care of interimplant distance maintenance to a 3-4mm.
• Implant insertion and confirmatory x-rays are performed.
• Gingival formers will be placed.
• Flap closure is performed with interrupted 4-0 polyproplene sutures.

Postoperative Care:

Postoperative medication -Administration of:

• Anti-inflammatory drugs (NSAIDS; Ibuprofen 600mg three times daily for 5 days) (Francesco Pieri et al, 2012).
• Antiseptic mouth rinse (0.12% Chlorhexidine oral rinse) will be prescribed starting from the second day for 60 seconds two times a day for 14 days (Jun Yu et al, 2015).

-Patient self-care instructions:

• Application of an ice bag to the treated area for the first 24 hours (Francesco Pieri et al, 2012).
• The patients were instructed to gently brush the operated area starting from the second day with a soft brush using roll technique.

Scheduled time of re-entry for patients:

3 months for prosthesis fabrication.

Clinical Examinations:

At the 3-month (T1), 6-month (T2) and 12-month (T3), the following clinical parameters will be recorded at the implant sites: Interimplant vertical papilla height, pink esthestic score (PES), probing depth (PD), peri-implant mucosal height (PMH), bleeding on probing at six sites of each implant (mesiobuccal, buccal, distobuccal, distolingual, lingual, and mesiolingual), and width of buccal keratinized mucosa (KM) at the midbuccal surface of each implant.

KM will be recorded as the linear distance from the mucosal margin to the mucogingival line.

Radiographic Examination Radiographic examination will be performed immediately after the surgical procedure (T0), and at T1 and T3. Standard periapical radiographs will be taken using a digital imaging software system.

Inclusion criteria

• Systemically healthy patients.
• Good oral hygiene.
• Missing minimum of two neighboring maxillary teeth with sufficient bucco-palatal bone of ≥ 6mm.
• Interimplant distance planned to be 3-4 mm.
• Patient acceptance of more than one year of follow up.

Exclusion criteria

• Vertically deficient ridges. (≤10 mm)
• Smokers.
• Pregnant females.
• Thin biotype