Evaluation of the Effect of Different Thread Designs on Primary Stability of Dental Implant Using Osseodensification Technique in Posterior Maxilla : Randomized Clinical Trial
1 other identifier
interventional
20
0 countries
N/A
Brief Summary
the aim of this study is to compare the primary stability of dental implant with knife threads design versus dental implant with double threads design using osseodensification technique in posterior maxilla .
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 Dec 2025
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
November 17, 2025
CompletedFirst Posted
Study publicly available on registry
November 21, 2025
CompletedStudy Start
First participant enrolled
December 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
November 21, 2025
November 1, 2025
9 months
November 17, 2025
November 17, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
primary stability of dental implant
measuring the primary stability using osstell device and smart peg
primary stability will be measured immediately after implant placement and 2nd record after 4 months
Secondary Outcomes (1)
marginal bone height changes
after 6 months of dental implant placement
Study Arms (2)
knife threads design dental implant
EXPERIMENTALthe intervention group is the knife threads dental implant using the osseodensification technique
double threads design dental implant
ACTIVE COMPARATORthe control group is the double threads dental implant using osseodensification technique
Interventions
Eligibility Criteria
You may qualify if:
- age from 20 to 60 years
- both sex
- patient with deficient width in posterior maxilla
You may not qualify if:
- inadequate oral hygiene
- smoking habit \> 10 cigarettes per day
- abuse of alcohol or drugs
- pregnancy
- local or systemic infection
- sever hepatic or renal dysfunction
- bony or soft tissue pathological condition at surgical site
- uncontrolled systemic diseases
- parafunctional habits
- inability or unwillingness to return for follow-up visits
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- dentist
Study Record Dates
First Submitted
November 17, 2025
First Posted
November 21, 2025
Study Start
December 1, 2025
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
November 21, 2025
Record last verified: 2025-11