NCT07442604

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

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2026

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

February 24, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 2, 2026

Completed
Last Updated

March 2, 2026

Status Verified

February 1, 2026

Enrollment Period

4 months

First QC Date

February 24, 2026

Last Update Submit

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

EXPERIMENTAL
Procedure: Densah burs

Magnetic Mallet group

EXPERIMENTAL
Procedure: Magnetic Mallet technique

Conventional Drilling group

EXPERIMENTAL
Procedure: Conventional Drilling technique

Interventions

Densah bursPROCEDURE

20 inserted dental implants by Densah burs into healed posterior maxillary alveolar ridge with an early loading pattern.

Densah burs group

20 inserted dental implants by Magnetic Mallet technique into healed posterior maxillary alveolar ridge with an early loading pattern.

Magnetic Mallet group

20 inserted dental implants by Conventional Drilling technique into healed posterior maxillary alveolar ridge with an early loading pattern.

Conventional Drilling group

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Conditions

Tooth Loss

Condition Hierarchy (Ancestors)

Periodontal DiseasesMouth DiseasesStomatognathic DiseasesTooth Diseases

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

Locations