Clinical Trials Logo

Clinical Trial Summary

This study was conducted to compare implant stability of Hiossen ET III implants with its new hydrophilic surface (NH) and Hiossen ET III implants with the SA surface.


Clinical Trial Description

Patients required at least two teeth to be rehabilitated with a fixed, implant-supported restoration, consecutively enrolled. Patients randomly received Sandblasted and Acid-etched (SA) surface implants (SA group) or SA implants with a newly developed bio-absorbable apatite nano coating (NH group). Outcome measures were: implant and prosthetic survival rate, complications, insertion torque, and implant stability quotient (ISQ) measured at implant placement and every week up to 8 weeks after implant placement. Comparison between groups was made by unpaired t test, while comparison between each follow-up will be made by paired t tests to detect any change during the follow-up. Complications and failures were compared by using Fisher exact test. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03649100
Study type Interventional
Source Osstem AIC
Contact
Status Completed
Phase N/A
Start date November 1, 2017
Completion date May 30, 2019

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
Active, not recruiting NCT05390996 - Implant Stability Changes In Dental Implants Installed By Osseodensification and Conventional Methods N/A