NCT07140887

Brief Summary

Teeth loss in the posterior mandible initiates residual ridge resorption especially in vertical direction, this causes difficulty in implant placement so ridge augmentation must be done either simultaneous with implant placement or in a staged approach Aim: To evaluate the effect of bone ring technique versus split bone block technique with simultaneous implant clinically on primary and secondary

Trial Health

87
On Track

Trial Health Score

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

Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2024

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

August 26, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 5, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 5, 2025

Completed
16 days until next milestone

First Submitted

Initial submission to the registry

August 21, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 26, 2025

Completed
Last Updated

August 26, 2025

Status Verified

August 1, 2025

Enrollment Period

11 months

First QC Date

August 21, 2025

Last Update Submit

August 21, 2025

Conditions

Keywords

Bone ring, trephine, piezotome, ridge augmentation, Khoury technique, implant

Outcome Measures

Primary Outcomes (3)

  • Change in implant stability

    Implant stability will be recorded immediately after placement (1ry stability) and after 6 months (2ry stability ) by using osstell device. The result is presented in form of ISQ value from 1to 100, the higher the ISQ the higher the stability of implant(

    Immediate and 6 months

  • Change in pain scores

    Pain will be assessed for 7 days postoperatively using 10-point visual analouge scale (VAS) (0-1=None, 2-4=mild, 5-7=moderate, 8-10=severe ).

    up to 7 days

  • Change in marginal bone level

    At buccal, lingual, mesial, and distal sites will be evaluated radiographically from the shoulder of the implant to the alveolar crest.

    6 and 9 months

Secondary Outcomes (2)

  • Change in bone density

    6 months

  • Change in edema

    up to 7 days

Study Arms (2)

Bone ring technique

EXPERIMENTAL
Other: Bone Ring

Split bone block technique

ACTIVE COMPARATOR
Other: Split Bone block

Interventions

Patients in this group will be treated with the bone ring technique. An implant drill will be used next to prepare central osteotomies corresponding to the final implant diameter to be placed in the center of the disc converting it to a "bone ring".

Bone ring technique

Patients of this group will be treated with split bone block with simultaneous implant technique. The bone shell will be split into two bone shells each 1 \~ 2 mm in thickness using a disc.

Split bone block technique

Eligibility Criteria

Age35 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients with missing posterior mandibular teeth.
  • Vertical bone defect from 3 to 4 mm.
  • Adequate zone of keratinized tissue.

You may not qualify if:

  • Presence of infection or periapical lesions in adjacent teeth.
  • Medically compromised patients with a condition that affects the procedure.
  • Insufficient inter-arch distance.
  • Bruxism or clenching.
  • Alcoholism.
  • Heavy Smokers.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Outpatient Clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University, Egypt

Alexandria, Azarita, 00203, Egypt

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 21, 2025

First Posted

August 26, 2025

Study Start

August 26, 2024

Primary Completion

August 5, 2025

Study Completion

August 5, 2025

Last Updated

August 26, 2025

Record last verified: 2025-08

Locations