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RecruitingNCT06477874Updated Jun 27, 2024

Assessment of Implants Placed in Consolidated Graft With Different Bone Drills.

An interventional study of Dental implants placement in Implant Complication and Bone Graft; Mechanical Complications, sponsored by Beni-Suef University. Recruiting at 1 site in Egypt. Open to participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2024-06-27.

Sponsored by Beni-Suef University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2025, 1 year 6 months ago, but the record still lists the study as recruiting.
  • Started Jun 2024; still recruiting 2 years 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

The anterior iliac crest is a popular source of bone harvest. However, when fused to the intramembranous jaw bones, it yields low-density bones that qualitatively and quantitatively endanger the fixture's stability.

In 1994, Summers first documented using the bone-condensing approach to improve the primary stability of dental implants.

This study aims to determine whether osseodensifying the consolidated mandibular bone grafts will improve implant stability and marginal bone loss

02

Conditions studied

  • Implant Complication
  • Bone Graft; Mechanical Complications

Keywords

  • Bone graft
  • Iliac crest
  • Implant stability
03

In context

Lead sponsor

Beni-Suef University is the lead sponsor of 333 studies on the registry; 116 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients of both sexes with an age range of 18-55 years.
  2. Patients subjected to a successful iliac crest mandibular bone graft after segmental mandibular resection.
  3. A minimal ridge height of ten millimeters and a ridge width of seven millimeters.
  4. Healthy soft tissue coverage, with a reasonable interaction space.

Exclusion criteria

Exclusion Criteria:

  1. Clinical or radiographic signs of graft infection, rejection, or massive resorption.
  2. The previous exposure to radiotherapy or chemotherapy.
  3. Any systemic disease that would affect bone healing or implant osseointegration.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
12 participants (estimated)

Study arms

  • Active comparator
    Test group

    The dental implants placed after bone osseodensification using densah burs

    Procedure: Dental implants placement

  • Active comparator
    Control group

    The dental implants placed after conventional bone drilling with the standard drills

    Procedure: Dental implants placement

Interventions

  • ProcedureDental implants placement

    implants placed in consolidated bone grafts

06

What researchers measure

Primary outcomes

  1. Radiographic bone loss

    Calibration of the amplitude of vertical bone loss

    Time frame: 6 months osseointegration period

Secondary outcomes

  1. Implant stability

    Calibration of primary and secondary implant stability quotient

    Time frame: 6 months osseointegration period

07

Study locations

1 of 1 sites recruiting
  • Department of Oral and Maxillofacial Surgery, Faculty of Oral and Dental Medicine, Modern University for Technology & Information.
    Cairo, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 27, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06477874
Lead sponsor
Beni-Suef University
Responsible party
Amr Gibaly (Associate Professor of Oral and Maxillofacial Surgery, Beni-Suef University) — Principal investigator
First posted
Jun 27, 2024
Start date
Jun 9, 2024
Primary completion
Apr 1, 2025 (estimated)
Completion
Apr 1, 2025 (estimated)
Last update
Jun 27, 2024

Study contacts

Maged Seleet, PHD
Contact
magedseleet@hotmail.com
01000367625

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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