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Ridge augmentation using titanium mesh and tenting screws in localized alveolar ridge deficiency

Clinical and radiographic assessment of protected bone augmentation using combination of autogenous and xenogenic bone graft with titanium mesh and tenting screws in management of localized alveolar ridge deficiency- A prospective in vivo study - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082505
Enrollment
12
Registered
2025-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge

Interventions

Intervention1: Protected bone augmentation in localized alveolar ridge deficiency: Clinical and radiographic evaluation of quantity of bone regeneration with the use of mixture of autogenous bone and

Sponsors

Government College of Dentistry Indore
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with localized combined alveolar ridge deficiency (horizontal and vertical) not involving more than 3 missing maxillary or mandibular teeth, either unilaterally or bilaterally Mild to moderate alveolar ridge deficiency with intraosseous ridge defects. 20-50 years of age of both sex and able to sign an informed consent. Maintainable oral hygiene. Who will be ready to have their progress followed for at least 6 months

Exclusion criteria

Exclusion criteria: Patients presenting with severe alveolar ridge deficiency with extraosseous defects. History of allergy or systemic diseases such as diabetes mellitus, immunocompromising diseases, blood dyscrasias, cardiovascular disease, renal disease etc. Patients with systemic medications like long term steroids, amino bisphosphonate therapy, anticoagulants, anticonvulsants, long term radiation therapy. Presence of active periodontal disease. Unwillingness to return for the follow up examination. Pregnancy or lactation, psychiatric illness Smokers and/or consuming tobacco in any

Design outcomes

Primary

MeasureTime frame
To clinically evaluate the amount of bone regenerated horizontally and vertically with the use of mixture of autogenous bone and xenogenic bone graft with titanium mesh along with tenting screws.Timepoint: Baseline (T0), 6months (T1)

Secondary

MeasureTime frame
To radiographically evaluate the amount of bone regenerated horizontally and vertically with the use of mixture of autogenous bone and xenogenic bone graft with titanium mesh along with tenting screws.Timepoint: Baseline (T0), Immediate post operative (T1), 6 months (T2)

Countries

India

Contacts

Public ContactDr Mitisha Anant Sawant

Government College of Dentistry

drshaleenk@gmail.com9827529603

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026