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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06254378
Other study ID # Sinus lifting
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 1, 2024
Est. completion date October 30, 2024

Study information

Verified date January 2024
Source Cairo University
Contact Amira R Elshikh, BCS
Phone 01068503398
Email Amira.raafat2512@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date October 30, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 80 Years
Eligibility 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%)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Sinus lifting with allograft
Participants will receive sinus lifting and allograft with immediate implant in premolar-molar area.
Other:
Sinus lifting without graft
Participants will receive sinus lifting with immediate implant in premolar-molar area without graft

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

References & Publications (2)

Fouad W, Osman A, Atef M, Hakam M. Guided maxillary sinus floor elevation using deproteinized bovine bone versus graftless Schneiderian membrane elevation with simultaneous implant placement: Randomized clinical trial. Clin Implant Dent Relat Res. 2018 Jun;20(3):424-433. doi: 10.1111/cid.12601. Epub 2018 Mar 25. — View Citation

Karagah A, Tabrizi R, Mohammadhosseinzade P, Mirzadeh M, Tofangchiha M, Lajolo C, Patini R. Effect of Sinus Floor Augmentation with Platelet-Rich Fibrin Versus Allogeneic Bone Graft on Stability of One-Stage Dental Implants: A Split-Mouth Randomized Clini — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Implant stability implant 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): During the implant placement procedure and after 6 months
Secondary Bone hight Newly formed bone length will be measured on cone beam ct by millimeter Before surgery and after 6 months