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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05390996
Other study ID # dental implant
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 5, 2022
Est. completion date January 2023

Study information

Verified date May 2022
Source University of Baghdad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the effect of Osseodensification on implant stability during the healing period The objective of this study is to compare between dental implant stability after osteotomy site preparation using osseodensification technique and conventional drilling technique immediately after implant installation (primary stability) , 6 week after the insertion of implant and 12 weeks later (secondary stability)


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 35
Est. completion date January 2023
Est. primary completion date September 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. medically fit patients = 18 years of age including both genders 2. alveolar ridges of sufficient vertical and horizontal dimensions 3. bone density less than 850 Hounsfield units (HU) which corresponds to D3-D5 bone density according to Misch bone classification based on preoperative CBCT findings Exclusion Criteria: 1. Patients with high bone density (more than 850 HU which corresponds to D1 and D2 according to Misch classification are not suitable for osseodensification. 2. Patient with severe buccal plate undercut or concavity 3. Active infection or inflammation in the implant zone 4. Presence of any uncontrolled systemic diseases. 5. Any patient need advance treatment such as sinus lifting and bone augmentation.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
dental implant placement
dental implant placement by using a different drilling techniques

Locations

Country Name City State
Iraq Baghdad University Baghdad Babalmatham

Sponsors (1)

Lead Sponsor Collaborator
University of Baghdad

Country where clinical trial is conducted

Iraq, 

Outcome

Type Measure Description Time frame Safety issue
Primary primary stability Mean implant stability between different comparators following implants insertion by using resonance frequency analysis scaled from 1 to 100 0 day (baseline)
Primary stability at the dip period Mean implant stability between different comparators following implants insertion by using resonance frequency analysis scaled from 1 to 100 6 week post surgery
Primary secondary stability Mean implant stability between different comparators following implants insertion by using resonance frequency analysis scaled from 1 to 100 12 week post surgery
See also
  Status Clinical Trial Phase
Completed NCT06148064 - EFFECT OF LOW-LEVEL LASER THERAPY ON STABILITY OF DENTAL IMPLANTS PLACED IN A FRESH EXTRACTED SOCKET N/A
Completed NCT03649100 - Osseointegration With a New Hydrophilic Surface N/A