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Sinus Lift With Hydroxyapatite Nano Particles Versus Tenting Technique

Not Applicable
Conditions
Maxillary Sinus Lift
Interventions
Procedure: sinus lift implant placement tenting
Procedure: sinus lift implant placement Hydroxyapatite Nano particles
Registration Number
NCT03177876
Lead Sponsor
Cairo University
Brief Summary

twenty recruited patients indicated for sinus augmentation and immediate implant placement will be divided into two groups (10 in each of the two groups), to compare bone formation and implant stability after shneiderian membrane elevation and augmentation with Hydroxyapatite Nano particles \[Nanostreams\] or augmentation with graft less tenting technique with simultaneous implant placement.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Patients with atrophic maxilla and pneumatization of the maxillary sinus with residual bone height at least 5mm of residual ridge as per MISCH criteria
  • Both sexes
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Exclusion Criteria
  • Sinus pathology
  • Heavy smokers more than 20 cigarettes per day
  • Patients with systemic disease that may affect normal healing
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
sinus lift implant placement tentingsinus lift implant placement tentingshneiderian membrane elevation and augmentation with graft less tenting technique with simultaneous implant placement
sinus lift implant placement Hydroxyapatite Nano particlessinus lift implant placement Hydroxyapatite Nano particlesshneiderian membrane elevation and augmentation with Hydroxyapatite Nano particles \[Nanostreams\] with simultaneous implant placement
Primary Outcome Measures
NameTimeMethod
patient satisfaction7 days post operative

evaluation of post operative complications in terms of pain and edema using patient pain chart

Secondary Outcome Measures
NameTimeMethod
height of bone gain or loss around the implant6 months post operative

two cone beam CT will be taken for the patients, one immediate post operative and the other 6 months post-operative then the amount of bone gained or loss will be assessed by superimposing the same section in the two cone beam CT

implant stabilitywill be measured intra-operative after implant insertion and will be measured one more time 6 months after the first operation at the time of implant exposure

measurement of the implant stability using osstell device

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