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Horizontal Bone AugmentationNCT06195761

Computer Guided Modified Ridge Splitting Versus Free Hand Technique in Horizontal Deficiency in Posterior Mandible

A study testing computer guided modified ridge splitting technique in horizontal bone deficiency in posterior mandible and free hand modified ridge splitting technique in horizontal bone deficiency in posterior mandible in people with Horizontal Bone Augmentation and Horizontal Ridge Deficiency, run by Cairo University at 1 site in Egypt.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

To assess the accuracy of the computer assessed guides in horizontal bone augmentation achieved at posterior mandible using guided modified ridge splitting technique versus free hand modified ridge splitting technique Read more about this study

Who is it for?
Ages 25 to 55 yearsHealthy volunteers can take part
What is being tested?
computer guided modified ridge splitting technique in horizontal bone deficiency in posterior mandible and free hand modified ridge splitting technique in horizontal bone deficiency in posterior mandible
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
18 participants
Where
1 siteEgypt
Study dates
15 May 2026to 15 Jun 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 55 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • posterior mandible with horizontal deficient alveolar ridge that is from 2 to 4 mm measured from the crest of the alveolar ridge buccolingually
  • Age range from 25-55 years. No sex predilection.
  • Patients free from any systemic conditions and bone metabolism diseases that might interfere with the surgical intervention, soft tissue or hard tissue healing.
  • Patients of adequate alveolar bone width.
  • Both genders males and females will be included
  • Normal vertical dimension with normal inter-arch space. The minimum number of missing teeth in the posterior mandible alveolar ridge is two adjacent anterior teeth

Who cannot join

  • Intra-bony lesions (e.g. cysts) or infections (e.g. abscess) that may retard the osteotomy healing.
  • Previous grafting procedures in the edentulous area.
  • General contraindications to implant surgery.
  • Subjected to irradiation in the head and neck area less than 1 year before implantation.
  • Untreated periodontitis.
  • Poor oral hygiene and motivation.
Show all 11Show fewer
  • Uncontrolled diabetes.
  • Pregnant or nursing.
  • Immunosuppressed or immunocompromised
  • Heavy smokers
  • Patients undergo medication interfere with bone healing

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Mina ElHadidi Sobhi Ramzi, BDS contact

+201225339712

mina.ramzi@dentistry.cu.edu.eg

Egypt1 site
  • Faculty of Dentistry - Cairo University

    Cairo, Manial, 12613

Other trials in Egypt

About this study

Official title: Radiographic Assessment of Computer Guided Modified Ridge Splitting Technique Versus Conventional Free Hand Technique in Management of Horizontal Deficiency in Posterior Mandible: a Randomized Control Clinical Trial

To assess the accuracy of the computer assessed guides in horizontal bone augmentation achieved at posterior mandible using guided modified ridge splitting technique versus free hand modified ridge splitting technique

Read the detailed description

The first treatment plan includes harvesting and fixing the bone graft in posterior mandibular area using a computer-modified surgical guide.

The second treatment plan includes manually harvesting and fixing the bone graft in posterior mandibular area without a surgical guide.

Being tested
computer guided modified ridge splitting technique in horizontal bone deficiency in posterior mandible, free hand modified ridge splitting technique in horizontal bone deficiency in posterior mandible
Keywords
computer guided modified ridge splitting, computer guided modified cortical shell technique, guided modified ridge splitting in posterior mandible

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • computer guided modified ridge splitting technique in horizontal bone deficiency in posterior mandibleProcedure or surgery

    Also called computer guided modified cortical shell technique

    treatment plan includes harvesting and fixing the bone graft in posterior mandibular area using a computer-modified surgical guide

  • free hand modified ridge splitting technique in horizontal bone deficiency in posterior mandibleProcedure or surgery

    Also called conventional modified cortical shell technique

    treatment plan includes manually harvesting and fixing the bone graft in posterior mandibular area without a surgical guide.

Study groups in NCT06195761
Study groupRoleWhat they receive
computer guided modified ridge splitting technique (study group)ExperimentalThe first treatment plan includes harvesting and fixing the bone graft in posterior mandibular area using a computer-modified surgical guide.
Receives: Procedure: computer guided modified ridge splitting technique in horizontal bone deficiency in posterior mandible
conventional modified ridge splitting technique (control group)ExperimentalThe second treatment plan includes manually harvesting and fixing the bone graft in posterior mandibular area without a surgical guide
Receives: Procedure: free hand modified ridge splitting technique in horizontal bone deficiency in posterior mandible

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Accuracy of the Computer Assessed Guide in the study group

    Accuracy of the Computer Assessed Guide in the study group In comparison with the control group between predicted and immediately postoperative horizontal bone width with Cone beam computed tomography in Millimeters measurement tool is CBCT scan superimposition in mm

    Measured: immediately postoperative

Secondary outcomes (1)
  1. Alveolar ridge horizontal bone gain

    measure the amount of horizontal bone width gaining by postoperative cone beam computed tomography in millimeters measurement tool is CBCT scan superimposition in mm

    Measured: 4 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Jan 2024
  2. Study start15 May 2026 (estimated)
  3. Primary completion15 May 2026 (estimated)
  4. Study completion15 Jun 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
treatment plan includes harvesting and fixing the bone graft in posterior mandibular area using a computer-modified surgical guide
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
18 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06195761
Sponsor's protocol ID
computer guided modified ridge
Status last verified
Jan 2026
First submitted
23 Dec 2023
Last updated
16 Jan 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Al-Ani O, Nambiar P, Ha KO, Ngeow WC. Safe zone for bone harvesting from the interforaminal region of the mandible. Clin Oral Implants Res. 2013 Aug;24 Suppl A100:115-21. doi: 10.1111/j.1600-0501.2011.02393.x. Epub 2012 Jan 11.

    PubMed 22233422
  • Sanchez-Labrador L, Molinero-Mourelle P, Perez-Gonzalez F, Saez-Alcaide LM, Brinkmann JC, Martinez JL, Martinez-Gonzalez JM. Clinical performance of alveolar ridge augmentation with xenogeneic bone block grafts versus autogenous bone block grafts. A systematic review. J Stomatol Oral Maxillofac Surg. 2021 Jun;122(3):293-302. doi: 10.1016/j.jormas.2020.10.009. Epub 2020 Nov 5.

    PubMed 33161168
  • De Stavola L, Fincato A, Bressan E, Gobbato L. Results of Computer-Guided Bone Block Harvesting from the Mandible: A Case Series. Int J Periodontics Restorative Dent. 2017 Jan/Feb;37(1):e111-e119. doi: 10.11607/prd.2721.

    PubMed 27977816
  • Schwartz-Arad D, Levin L, Sigal L. Surgical success of intraoral autogenous block onlay bone grafting for alveolar ridge augmentation. Implant Dent. 2005 Jun;14(2):131-8. doi: 10.1097/01.id.0000165031.33190.0d.

    PubMed 15968184
  • Assaf A, Saad M, Daas M, Abdallah J, Abdallah R. Use of narrow-diameter implants in the posterior jaw: a systematic review. Implant Dent. 2015 Jun;24(3):294-306. doi: 10.1097/ID.0000000000000238.

    PubMed 25851960

Questions about this trial

What is this clinical trial studying?

A study testing computer guided modified ridge splitting technique in horizontal bone deficiency in posterior mandible and free hand modified ridge splitting technique in horizontal bone deficiency in posterior mandible in people with Horizontal Bone Augmentation and Horizontal Ridge Deficiency, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 16 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Mina ElHadidi Sobhi Ramzi, BDS (+201225339712, mina.ramzi@dentistry.cu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Accuracy of the Computer Assessed Guide in the study group (time frame: immediately postoperative). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06195761, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jan 2026.

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