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Evaluation of the Efficacy of Allograft Versus Tenting Technique in Open Sinus Lifting With Immediate Implant Placement

Evaluation of the Efficacy of Allograft Versus Tenting Technique in Open Sinus Lifting With Immediate Implant Placement A Randomized Clinical Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06254378
Enrollment
20
Registered
2024-02-12
Start date
2024-03-01
Completion date
2024-10-30
Last updated
2024-02-12

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

Conditions

Implant Complication, Sinus; Dental, Surgery-Complications

Brief summary

Implant placement in deficient posterior maxilla is a challenging clinical situation that necessitates appropriate treatment options to restore this area. -Aim of the study: To compare allograft vs tenting technique in terms of implant stability and bone height.

Detailed description

Rationale for carrying out the trial: The research population will be divided into two groups. Group1 will be treated by allograft with immediate implant technique, Group2 will be treated by tenting technique with immediate implant technique. Allograft has been effective in augmenting bone growth and has been proven to be a vital asset in sinus lifting.

Interventions

PROCEDURESinus lifting with allograft

Participants will receive sinus lifting and allograft with immediate implant in premolar-molar area.

OTHERSinus lifting without graft

Participants will receive sinus lifting with immediate implant in premolar-molar area without graft

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patient with missing upper pre molar , molar teeth 2. Patients in need of bone grafting of the maxillary sinus to house an implant. 3. Patients with residual alveolar crest of at least 3-4mm in height and 5mm in width distal to the canine as measured on CBCT scan 4. Patients with adequate inter-arch space

Exclusion criteria

1. Patients suffering from any sinus pathosis. 2. Patients who are heavy smokers (\>10 cigarettes/day). 3. Patient under psychiatric therapy or unrealistic expectations 4. Patients of systemic conditions that may interfere with carrying out the surgical procedure. 5. Lack of opposite occluding dentition/prosthesis in the area intended for implant placement 6. Severe bruxism or clenching 7. Poor oral hygiene (full mouth bleeding on probing and full mouth plaque index \>25%)

Design outcomes

Primary

MeasureTime frameDescription
Implant stabilityDuring the implant placement procedure and after 6 monthsimplant stability quotient(ISQ) is the evaluation unit set to determine the correct isq\<60:low stability isq 60-65 : medium stability isq \>70: high stability stability of the implant, this module by means of a resonance frequency analysis (rfa) applied to the bone manages to measure stability on an isq scale from 1 to 100 (khz):

Secondary

MeasureTime frameDescription
Bone hightBefore surgery and after 6 monthsNewly formed bone length will be measured on cone beam ct by millimeter

Contacts

Primary ContactAmira R Elshikh, BCS
Amira.raafat2512@gmail.com01068503398
Backup ContactSalma H Abdelaty
0 111 399 9772

Outcome results

None listed

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