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Radiographic Assessment of Bone Gain Following Sinus Lifting With Simultaneous Implant Placement Using Crestal Approach With Membrane Control Technique for Bone Augmentation of Atrophied Maxillary Posterior Ridge

Radiographic Assessment of Bone Gain Following Sinus Lifting With Simultaneous Implant Placement Using Crestal Approach With Membrane Control Technique for Bone Augmentation of Atrophied Maxillary Posterior Ridge

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06446687
Enrollment
10
Registered
2024-06-06
Start date
2024-06-01
Completion date
2025-02-01
Last updated
2024-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Implant Site Reaction, Maxillary Deficiency

Keywords

Closed Sinus lifting, Bone Gain

Brief summary

This study aims to evaluate the quantity and quality of the native and the newly bone around dental implants that's simultaneously installed with sinus lifting

Interventions

PROCEDUREDental implant with sinus lifting.

Surgery will be performed under local infiltration anaesthesia. Flap will be done. For maxillary sinus lifting by using Crestal approach with Membrane Control Technique by Wang (Wang, 2017) will be employed. After reflecting on the flap, Magic Split will be used to confirm bone quality clinically. This will be followed by site preparation using Magic Marking Drill. Bone drilling will then be performed by Magic Drill shorter by 2 mm from the sinus floor. This will be followed by sinus lifting by using Magic Sinus Lifter (MSL). The 3mm space of the apex of the Sinus Lifter instrument enables direct control of the bone-block and consequently the membrane, which is connected to the bone-block. the fixture will be installed in the conventional method. Then cover the fixture with the cover screw. The flap will be sutured. An immediate CBCT will be requested to ensure the implant is in its proper position.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients required dental implant treatment in the posterior maxilla, in the premolar and molar regions ( both sexes). 2. Residual bone height 4-8mm in the estimated implant positions. 3. The bone width of the alveolar ridge is at least 5mm in estimated implant positions. 4. The edentulous ridges are covered with optimal thickness of mucoperiosteum.

Exclusion criteria

1. Patients with a systemically diseases or inflammation whether local or generalized. 2. Patients with bleeding disorders. 3. Subjected to irradiation in the head and neck area less than 1 year before implantation. 4. Poor oral hygiene and motivation. 5. Pregnant or nursing. 6. Severe bruxism or clenching. 7. Active infection or severe inflammation in the area intended for implant placement. 8. Unable to open mouth sufficiently to accommodate the surgical tooling.

Design outcomes

Primary

MeasureTime frameDescription
Cone beam computed tomography (CBCT) bone height formation around dental implantsPatients will be evaluated after 3 days and weekly for the first month and then once monthly up to 4 months for signs of dehiscence. then cone-beam computed tomography 4 months postoperatively to calculate the amount of vertical bone gain.Calculate bone height and formation around dental implants.

Secondary

MeasureTime frameDescription
Cone beam computed tomography (CBCT) density formation around dental implantsPatients will be evaluated after 3 days and weekly for the first month and then once monthly up to 4 months for signs of dehiscence. then cone-beam computed tomography 4 months postoperatively to calculate the amount of vertical bone gain.Calculate bone density formation around dental implants.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026