Comparative Assessment of Primary Stability in Double, and Triple Thread Implant Designs
1th stability
1 other identifier
interventional
20
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 17, 2026
CompletedFirst Posted
Study publicly available on registry
August 20, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 30, 2027
August 26, 2026
August 1, 2026
4 months
August 17, 2026
August 24, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants assigned to this arm will receive a double-thread dental implant in the posterior maxilla
Triple-thread implant
EXPERIMENTALParticipants 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).
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).
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).
Eligibility Criteria
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
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
- 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