Not yet recruiting NCT07079917
Alveolar Ridge Augmentation Using Minimally Invasive Subperiosteal Tunneling With Xenogenic Bone Graft and PRF
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: subperiosteal tunneling for horizontal alveolar ridge augmentation, conventional alveolar ridge augmentation.
- Who it may be relevant to
- Registry conditions: Alveolar Bone Loss. Basic parameters: 18 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Alveolar Ridge Augmentation Using Minimally Invasive Subperiosteal Tunneling With Xenogenic Bone Graft and Platelet-Rich Fibrin: Randomized Controlled Trial
Overview
surgical horizontal augmentation for maxillary alveolar ridge using minimally invasive subperiosteal tunneling in comparison to conventional surgical technique
Interventions
- Procedure subperiosteal tunneling for horizontal alveolar ridge augmentation
subperiosteal dissection through horizontal incision only - Procedure conventional alveolar ridge augmentation
horizontal alveolar ridge augmentation through trapezoidal flap
Primary outcome measures
- Maxillary alveolar bone width [Time frame: 6 months]
Eligibility criteria
Inclusion criteria
- Adults over 18 years old seeking an implant-supported restoration with deficient horizontal posterior maxillary alveolar ridge, at area of one or two missed teeth of less than 5 mm buccolingual width.
- Minimum vertical height of 8 mm.
- Gingival tissue of healthy adequate keratinization, more than 2mm.
Exclusion criteria
- The presence of uncontrolled diabetes or any other systemic condition which may complicate the surgical procedure or interfere with bone healing
- Radiotherapy to the head and neck region
- Chemotherapy within the last 12 months
- Uncontrolled periodontitis
- Smoking
- Bisphosphonate therapy
- Pregnancy
- Presence of periapical infection or lesion
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Fayoum University — Al Fayyum
Identifiers
NCT: NCT07079917 · will be ready at end of study