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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04442763
Other study ID # Sara89
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2022
Est. completion date August 2023

Study information

Verified date April 2022
Source Cairo University
Contact Sara Abdel Raouf, Assistant Researcher
Phone +201001271266
Email sara.zagharii@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Implants will be placed in posterior maxilla using two drilling methods; the osseodensification technique and standard drilling protocols. Implant stability will be measured right after implant placement and after 3 months. crestal bone level will be measured after implant placement and after 3 and 9 months.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date August 2023
Est. primary completion date August 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Age: >18 years; - Partially edentulous patients in maxillary posterior area (premolar-molar area) - Sufficient ridge height - Sufficient ridge width - Adequate soft tissue biotype. - Patients with adequate inter-arch space for placement of implant prosthetic part. - Good oral hygiene - Patients who accept to sign an informed consent. Exclusion Criteria: - Systemic diseases that contraindicate implant placement, surgical procedures or may impair normal healing - Patients with habits that may jeopardize the implant longevity as alcoholism and parafunctional habits. - History of radiation therapy to the head and neck - Bone augmentation to implant site - Heavy smokers (= 10 cigarettes per day). - Pregnant females - Psychiatric problems

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Densah Burs
osseodensification method
Standard drills
conventional drilling

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Implant stability Implant stability will be measured using Osstell (Resonance Frequency Analysis). the measurement unit is Implant stability quotient (ISQ) (range 1-100) baseline- 3 months
Secondary Crestal bone level Digital radiographs baseline- 3 months- 9 months
See also
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Completed NCT04345133 - Effect of Undersized Drilling Upon the Immediate Implants N/A
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