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Non-grafted Maxillary Sinus Floor Elevation With Simultaneous Implant Placement Using Different Implant Lengths

Non-grafted Maxillary Sinus Floor Elevation With Simultaneous Implant Placement Using Different Implant Lengths

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03731650
Enrollment
20
Registered
2018-11-06
Start date
2019-01-01
Completion date
2019-08-15
Last updated
2018-11-06

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

Conditions

Maxillary Sinus Lift

Brief summary

twenty recruited patients indicated for sinus augmentation and simultaneous implant placement will be divided into two groups (10 in each of the groups).to evaluate & compare bone formation & implant stability after shneiderian membrane elevation and augmentation with graft less tenting technique with different implant lengths. group one will receive 8mm implant lenght while group two will receive 10mm implants.

Interventions

non grafted maxillary sinus floor augmentation with simultaneous implant placement

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* patient with atrophic maxilla & pneumatized maxillary sinus with residual bone height at least 4mm of residual ridge * both sexes

Exclusion criteria

* patients with systematic diseases that may affect normal healing * sinus pathology * heavy smokers more than 20 cigarettes per day

Design outcomes

Primary

MeasureTime frameDescription
height of gained bone6 months post operativetwo cone beam CT will be done for the patients, one immediate post operative & the other 6 months post operative then the amount of gained bone will be assessed by superimposing the same section in the two cone beam CT.

Secondary

MeasureTime frameDescription
implant stabilitywill be measured intra operative after implant insertion and will be measured once more 6 months post operative after the first operation at the time of implant exposuremeasurement of the implant stability using OSSTELL device.

Contacts

Primary Contactahmed abdul nasser ali, BDS
ahmedabdulnasserali@gmail.com00201115905965
Backup Contactahmed abdel rahman mohammed, MDS
airplayer2003@yahoo.com00201005261204

Outcome results

None listed

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