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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03661957
Other study ID # cairo university 99
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 2018
Est. completion date April 2019

Study information

Verified date September 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assessment the need for sinus floor elevation when restoring atrophic posterior maxilla or it will be enough to use of short implant


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date April 2019
Est. primary completion date December 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria:

- Patients with partially edentulous in the posterior area of the maxilla, with a residual ridge that allowed insertion of =8 mm length implants.

- Both sexes.

- No intraoral soft and hard tissue pathology

- No systemic condition that contraindicate implant placement.

Exclusion Criteria:

- Sinus pathology.

- Heavy smokers more than 20 cigarettes per day.

- Patients with systemic disease that may affect normal healing.

- Psychiatric problems

- Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site

- Immunodeficiency pathology, bruxism, stress situation (socially or professionally), emotional instability, and unrealistic aesthetic demands.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Non grafted maxillary sinus floor elevation with simultaneous implant placement
lateral window for sinus elevation ,membrane elevation ,implant placement , membrane for window closure
using short dental implants for posterior atrophic maxilla
placement of short dental implant with bone height below 8mm

Locations

Country Name City State
Egypt Ahmed Maher Mansour Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary primary stability measuring primary stability using osstel 6 months
Secondary marginal bone loss measuring marginal bone loss using cone beam ct 6 months
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