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Sinus Lift With Hydroxyapatite Nano Particles Versus Tenting Technique

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Maxillary Sinus Lift

Treatments

Procedure: sinus lift implant placement Hydroxyapatite Nano particles
Procedure: sinus lift implant placement tenting

Study type

Interventional

Funder types

Other

Identifiers

NCT03177876
cebc.cairo university

Details and patient eligibility

About

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.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Exclusion criteria

  • Sinus pathology
  • Heavy smokers more than 20 cigarettes per day
  • Patients with systemic disease that may affect normal healing

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

sinus lift implant placement Hydroxyapatite Nano particles
Experimental group
Description:
shneiderian membrane elevation and augmentation with Hydroxyapatite Nano particles \[Nanostreams\] with simultaneous implant placement
Treatment:
Procedure: sinus lift implant placement Hydroxyapatite Nano particles
sinus lift implant placement tenting
Active Comparator group
Description:
shneiderian membrane elevation and augmentation with graft less tenting technique with simultaneous implant placement
Treatment:
Procedure: sinus lift implant placement tenting

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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