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Randomized Trial of Five Implant Osteotomy Protocols on Stability and Anxiety

NCT07234214 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-11-18

No results posted yet for this study

Summary

This clinical trial is studying different methods of preparing bone for dental implants. When a tooth is missing, a small titanium screw called a dental implant can be placed in the jaw to replace it. The stability of the implant during the first weeks after surgery is very important for long-term success.

In this study, 100 patients each received a single dental implant. They were randomly assigned to one of five surgical methods: drilling at 50, 300, or 800 revolutions per minute (rpm), bone densification using special burs, or bone condensation using condenser drills. The goal was to compare how these techniques affect implant stability, measured by insertion torque and resonance frequency analysis, as well as the patient's anxiety before and after surgery.

This research aims to find which technique provides the best balance between bone healing and patient comfort. All participants were healthy adults, and the study was approved by the institutional ethics committee.

Conditions

  • Dental Implant Surgery
  • Osteotomy Protocols

Interventions

PROCEDURE

Osteotomy technique - 50 Rpm

Ultra-low-speed sequential drilling at 50 rpm without irrigation.

PROCEDURE

Osteotomy technique - 300 Rpm

Moderate-speed sequential drilling at 300 rpm with irrigation.

PROCEDURE

Osteotomy technique - 800 Rpm

High-speed sequential drilling at 800 rpm with irrigation.

PROCEDURE

Osteotomy technique - DNS (Osseodensification)

Osseodensification using Densah® burs at 1200 rpm counterclockwise with irrigation.

PROCEDURE

Osteotomy technique - CDS (Bone Condensation)

Bone condensation with condenser drills at 50 rpm clockwise without irrigation.

Sponsors & Collaborators

  • Sercan Küçükkurt

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
78 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-09-01
Primary Completion
2023-05-01
Completion
2023-05-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07234214 on ClinicalTrials.gov