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Atrophic MandibleNCT07884630

Horizontal Ridge Augmentation in Atrophic Posterior Mandible With Delayed Implant Placement

A study testing atrophied ridge augmentation in people with Atrophic Mandible, run by Mansoura University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study will assess the clinical and radiographic outcomes of tenting pole technique versus modified tunneling technique used for horizontal augmentation of atrophied posterior mandibular ridge associated with delayed implant placement. Read more about this study

Who is it for?
Ages 18 to 45 yearsHealthy volunteers can take part
Conditions the study is for
Atrophic Mandible
What is being tested?
atrophied ridge augmentation
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
1 siteEgypt
Study dates
1 Nov 2023to 5 Mar 2025
Phase
Interventional
Are there results?
None posted in the registry

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 18 to 45 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 1. Patient age 18-45 years old. 2. Cooperative patient with high motivation and acceptable oral hygiene. 3. Mandibular posterior narrow ridge with width 3-5 mm bucco-lingually. 4. Bone height allowing the insertion of at least 8 mm of implant length without the need for vertical augmentation.
  • 5. No deep undercut at the ridge in the buccal aspect. 6. Presence of enough amount of keratinized gingiva. 7. Favorable occlusion and no parafunctional habits. 8. Patients able to comply with the required recall visits.

Who cannot join

  • 1. General contraindications for dental and/or surgical treatments. \ 2. Concurrent or previous radiotherapy of head area. 3. Smokers. 4. Pregnancy.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Dentistry

    Al Mansurah

Other trials in Egypt

About this study

Official title: "Different Surgical Techniques for Horizontal Ridge Augmentation in Atrophic Posterior Mandible for Delayed Implant Placement", Which One is More Stable? A Randomized Clinical Trial

The study will assess the clinical and radiographic outcomes of tenting pole technique versus modified tunneling technique used for horizontal augmentation of atrophied posterior mandibular ridge associated with delayed implant placement.

Read the detailed description

Clinically, the greatest loss of the alveolar ridge is usually in the horizontal dimension.1 Horizontal bone augmentation is a necessary and indispensable procedure for successful implant placement in a narrow alveolar ridge. A variety of reconstructive approaches have been introduced in order to obtain adequate bone volume prior to implant placement such as guided bone regeneration (GBR),2 ridge split/expansion,3 block grafting,4 tenting pole technique5 and tunneling technique.6

Autogenous block grafting or onlay bone grafts harvested either extraorally from the hip, tibia, clavarium and iliac crest or intraorally from maxillary tuberosity, symphysis of the chin, mandibular ramus and external oblique ridge. All these methods are associated with morbidity of donor sites, resorption of materials, and increased treatment costs. Hence various alternative procedures were developed to minimize this morbidity.3

On the other hand, splitting and expanding the edentulous ridge for bone augmentation and implant placement was considered as an innovative technique as it avoids the need for a second surgical site which further reduces the ailment of the patient.7 Historically bone splitting technique is used to increase the width of bone by splitting and expansion of the existing residual ridge.8 Bone splitting technique was developed by Simion et al.9 and Scipioni et al.8 In the early 1990s. Simion et al.9 aimed at originating a ''self-space making defect'' by separating the buccal cortical bone of narrow alveolar crests in two parts through a longitudinal greenstick fracture to create a gap for dental implants insertion.

GBR has demonstrated a predictable result in lateral augmentation and long-term implant success. To avoid shrinkage resulting from pressure after flap closure, several space-maintenance modalities were used to facilitate formation of reconstructed ridge such as tenting screws,10 titanium (Ti) meshes,11 and Ti-reinforced polytetrafluoroethylene (PTFE) membranes.12

Basically nonresorbable membranes have a high risk of exposure, necessitating removal in the re-entry stage.12 Incontrary, resorbable membranes have shown better biocompatibility and support of underneath bone growth.13 However, their lack of stiffness can lead to decreased bone volume gain. Therefore, the tent-pole technique, which combines resorbable collagen membrane and tenting screws, represents an effective approach, offering easy manipulation and low complication rates. 13

Tenting of mucoperiosteum has shown good potential in the rehabilitation of atrophied alveolar ridges. Expansion of the soft tissue with the use of titanium mini-screws and guided bone regeneration was introduced by Bash Le et al., 2010.10 They evaluated "the use of titanium screws in tenting fashion that was surrounded by particulate human mineralized allograft to reconstruct large mandibular defects before implant placement".

One of the techniques of guided bone regeneration is subperiosteal tunneling, suggested by Kent et al.14 In this technique, two vertical incisions are created in the ridge, and the area between them is totally detached, forming a tunnel. The graft material is positioned, and the area is sutured.15,16This allows the bone graft to be covered by an intact periosteum.17 Because of its minimal invasiveness, this technique has a shorter surgical time and lower postoperative morbidity.18-20

However, subperiosteal tunneling technique is a partially blind procedure that requires patience and delicate surgical maneuvers to develop the subperiosteal flap that could form a pocket for graft materials. Though this bone augmentation does not permit a direct view of the deficient ridge. Meanwhile, it has advantages of less postoperative complications such as less bleeding, discomfort, bone loss, and surgery recovery time. Moreover, augmentation without application of fixation is still controversial.21,22

According to forementioned data, this study will be directed to assess the clinical and radiographic outcomes of tenting pole technique versus modified tunneling technique used for horizontal augmentation of atrophied posterior mandibular ridge associated with delayed implant placement.

Being tested
atrophied ridge augmentation
Keywords
atrophied ridge, augmentation, dental implant

What participants receive

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

  • atrophied ridge augmentationProcedure or surgery

    non invasive ridge augmentation techniques

Study groups in NCT07884630
Study groupRoleWhat they receive
ridge splittingOtherridge splitting and expansion for lower posterior atrophied ridge and implant placement after 6 months
Receives: Procedure: atrophied ridge augmentation
tenting pole techniqueOthertenting pole technique for lower posterior atrophied ridge and implant placement after 6 months
Receives: Procedure: atrophied ridge augmentation
tunnling techniqueOthertunnling technique for lower posterior atrophied ridge and implant placement after 6 months
Receives: Procedure: atrophied ridge augmentation

What is being measured

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

  1. bone width gain and loss

    • Bone width of the surgical site (alveolar bone) will be measured for every planed implant site from the outermost buccal surface of bone to the outermost lingual surface of bone at four different levels - alveolar bone crest, 2mm, 4mm and at 6mm apical to the crest.

    Measured: 6 months after augmentation and 6 months after implant placement

Timeline

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

  1. First posted20 Oct 2026
  2. Study start1 Nov 2023
  3. Primary completion20 Jan 2025
  4. Study completion5 Mar 2025

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
The patients in this trial were split into three groups: * Group I: In which the ridge splitting technique was used for horizontal ridge augmentation with delayed implant placement. * Group II: In which the tenting pole technique was used for horizontal ridge augmentation with delayed implant placement. * Group III: In which the modified tunneling technique was used for horizontal ridge augmentation with delayed implant placement.
Masking
None (open label)
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07884630
Sponsor's protocol ID
horizontal ridge augmentation
Status last verified
Oct 2026
First submitted
13 Oct 2026
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing atrophied ridge augmentation in people with Atrophic Mandible, run by Mansoura 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 2 inclusion and 1 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: finished, as of the sponsor's last update on 20 Oct 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

bone width gain and loss (time frame: 6 months after augmentation and 6 months after implant placement). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 20 Oct 2026.

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