NCT07775443

Brief 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

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
4mo left

Started Sep 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress22%
Sep 2026Jan 2027

First Submitted

Initial submission to the registry

August 17, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 20, 2026

Completed
12 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2027

Last Updated

August 26, 2026

Status Verified

August 1, 2026

Enrollment Period

4 months

First QC Date

August 17, 2026

Last Update Submit

August 24, 2026

Conditions

Keywords

dental implantprimary implant stabilityprimary stabilitythread designdouble threadtriple thread

Outcome Measures

Primary Outcomes (1)

  • insertion torque

    The primary outcome of this study will be the insertion torque, expressed in Newton-centimeter (Ncm). Measurements will be performed using a surgical motor/torque wrench and recorded at the time of implant placement (T0).

    at the time of implant placement T0

Secondary Outcomes (1)

  • implant stability (ISQ)

    3 months

Study Arms (2)

Double-Thread Implant Group

EXPERIMENTAL

Participants assigned to this arm will receive a double-thread dental implant in the posterior maxilla

Device: double thread dental implant

Triple-thread implant

EXPERIMENTAL

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: triple thread dental implant

Interventions

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).

Triple-thread 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).

Double-Thread Implant Group

Eligibility Criteria

Age20 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients aged 20-55 years.
  • Medically healthy individuals without any systemic disease that affects bone healing (e.g., uncontrolled diabetes, osteoporosis).
  • Patients requiring dental implants in the posterior maxilla.
  • Adequate bone volume for implant placement.
  • Signed informed consent for participation in the study.

You may not qualify if:

  • Smokers (due to the potential negative impact on bone healing and implant success).
  • Pregnant or breastfeeding women.
  • Patients with a history of radiotherapy or chemotherapy.
  • Patients with severe periodontal disease.
  • Individuals with a history of allergic reactions to implant materials.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

falah M Alshahrani, BDS

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
Participants will be blinded to the type of implant thread design received. The investigator will not be blinded because the investigator performs the implant placement and measures implant stability.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: participants will be randomly assigned to two parallel groups. One group will receive double-thread dental implants, while the other group will receive triple-thread dental implants. Primary implant stability will be compared between the two groups
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
masters candidate

Study Record Dates

First Submitted

August 17, 2026

First Posted

August 20, 2026

Study Start

September 1, 2026

Primary Completion (Estimated)

December 30, 2026

Study Completion (Estimated)

January 30, 2027

Last Updated

August 26, 2026

Record last verified: 2026-08