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.
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.
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.
- Conditions
- Atrophic Mandible
- 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 group | Role | What they receive |
|---|---|---|
| ridge splitting | Other | ridge splitting and expansion for lower posterior atrophied ridge and implant placement after 6 months Receives: Procedure: atrophied ridge augmentation |
| tenting pole technique | Other | tenting pole technique for lower posterior atrophied ridge and implant placement after 6 months Receives: Procedure: atrophied ridge augmentation |
| tunnling technique | Other | tunnling 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.
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.
- First posted20 Oct 2026
- Study start1 Nov 2023
- Primary completion20 Jan 2025
- Study completion5 Mar 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Atrophic MandibleStudies of the same condition, open and under way.
- More trials run by Mansoura UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Mansoura University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 20 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT07884630
- Acronym / sponsor ID
- horizontal ridge augmentation
- Conditions
- Atrophic Mandible
- Keywords
- atrophied ridge, augmentation, dental implant
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 15 participants (actual)
- Lead sponsor
- Mansoura UniversityUniversity, hospital or other
- Study start
- 1 Nov 2023 (actual)
- Primary completion
- 20 Jan 2025 (actual)
- Study completion
- 5 Mar 2025 (actual)
- First posted
- 20 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- 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.
| Arm | Type | Receives |
|---|---|---|
| ridge splitting | Other | Procedure: atrophied ridge augmentationridge splitting and expansion for lower posterior atrophied ridge and implant placement after 6 months |
| tenting pole technique | Other | Procedure: atrophied ridge augmentationtenting pole technique for lower posterior atrophied ridge and implant placement after 6 months |
| tunnling technique | Other | Procedure: atrophied ridge augmentationtunnling technique for lower posterior atrophied ridge and implant placement after 6 months |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- 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.
Key exclusion criteria (1 listed)
- 1. General contraindications for dental and/or surgical treatments. \ 2. Concurrent or previous radiotherapy of head area. 3. Smokers. 4. Pregnancy.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| atrophied ridge augmentationnon invasive ridge augmentation techniques | Procedure or surgery | ridge splitting, tenting pole technique, tunnling technique |
Primary outcome
bone width gain and loss
Time frame: 6 months after augmentation and 6 months after implant placement
- 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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Oct 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.