MedTrace Logo

Comparative Assessment of Primary Stability in Double, and Triple Thread Implant Designs

NCT07775443 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2026-08-26

No results posted yet for this study

Summary

The goal of this randomized clinical trial is to compare the primary stability of double-thread and triple-thread dental implant designs in patients requiring implant placement in the posterior maxilla.

The main question it aims to answer is whether implant thread design influences primary implant stability in the posterior maxilla.

Participants will be randomly assigned to one of two groups. Group A will receive a double-thread dental implant, while Group B will receive a triple-thread dental implant. Primary implant stability will be assessed at the time of implant placement using insertion torque and resonance frequency analysis (ISQ).implant stability using ISQ will also be evaluated at 3 months

Conditions

  • Dental Implant
  • Primary Stability of the Implants

Interventions

DEVICE

triple thread dental implant

Participants assigned to this group will receive a triple-thread dental implant placed in the posterior maxilla. Primary implant stability will be assessed at the time of implant placement using insertion torque and resonance frequency analysis (ISQ).

DEVICE

double thread dental implant

Participants assigned to this group will receive a double-thread dental implant placed in the posterior maxilla. Primary implant stability will be assessed at the time of implant placement using insertion torque and resonance frequency analysis (ISQ).

Sponsors & Collaborators

  • Future University in Egypt

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-09-01
Primary Completion
2026-12-30
Completion
2027-01-30

More Related Trials

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 NCT07775443 on ClinicalTrials.gov