Implant Stability Changes Using Different Technique in Posterior Maxilla With Early Loading Protocol
1 other identifier
interventional
60
1 country
1
Brief Summary
60 implants were placed in patients seeking implantation of their lost posterior maxillary teeth (premolar and molars) with normal bone height beneath the floor of the maxillary sinus. The patients were selected from those attending the outpatient clinic of the Oral \& Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University. 60 implants will be randomly and uniformly divided into two equal groups: Group 1: It was consisted of 20 inserted dental implants by Densah burs into healed posterior maxillary alveolar ridge with an early loading pattern. Group 2: It was consisted of 20 inserted dental implants by Magnetic Mallet technique into healed posterior maxillary alveolar ridge with an early loading pattern. Group 3: It was consisted of 20 inserted dental implants by Conventional Drilling technique into healed posterior maxillary alveolar ridge with an early loading pattern.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
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
Study Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2026
CompletedFirst Submitted
Initial submission to the registry
February 24, 2026
CompletedFirst Posted
Study publicly available on registry
March 2, 2026
CompletedMarch 2, 2026
February 1, 2026
4 months
February 24, 2026
February 27, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Implant stability
Implant stability was assessed at the time of implant insertion, 1 month and 2 months after surgery. The analysis of resonance frequency analysis (RFA) was made using an Osstell Mentor apparatus. The smart peg was attached to the dental implant. The RFA value was measured 4 times in 4 directions (every 90°). The results were expressed as implant stability quotient (ISQ) and averaged for each implant. The ISQ scale ranges from 0 to 100. The values less than 60 indicate low implant stability, values from 60 to 69 indicate medium stability, while values from 70 to 79 indicate high stability.
2 months
Study Arms (3)
Densah burs group
EXPERIMENTALMagnetic Mallet group
EXPERIMENTALConventional Drilling group
EXPERIMENTALInterventions
20 inserted dental implants by Densah burs into healed posterior maxillary alveolar ridge with an early loading pattern.
20 inserted dental implants by Magnetic Mallet technique into healed posterior maxillary alveolar ridge with an early loading pattern.
20 inserted dental implants by Conventional Drilling technique into healed posterior maxillary alveolar ridge with an early loading pattern.
Eligibility Criteria
You may qualify if:
- Patient with missing one or more posterior maxillary teeth.
- Patients in the age group between 18 and 60 years old.
- mm or more vertical bone height is present.
- No gender preface in selection of the patients.
- Good oral hygiene.
- Non-smokers.
- Patients willing to be present during the study follow up intervals.
- Patients free from any systemic diseases.
- mm or more ridge width is present.
- Crown height space of at least 8 mm.
- Patients without any para-functional habits (bruxism and clenching).
You may not qualify if:
- Patients with any pathological lesion or root tips at the planned surgical site.
- Patients with systemic diseases that contra-indicate the surgical procedure or affect bone healing process such as uncontrolled diabetes mellitus, bleeding disorders, serious osseous disorders, and mental disorders.
- Patient taking drugs that could affect bone healing process as in immunosuppressive drugs and bisphosphonates.
- Alcoholism.
- Untreated periodontal disease or bad oral hygiene.
- Pregnancy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Heba elsheikh
Al Mansurah, 002, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 24, 2026
First Posted
March 2, 2026
Study Start
October 1, 2025
Primary Completion
February 1, 2026
Study Completion
February 1, 2026
Last Updated
March 2, 2026
Record last verified: 2026-02