Alveolar Ridge Augmentation Using Minimally Invasive Subperiosteal Tunneling With Xenogenic Bone Graft and PRF

NCT07079917 · tracked via the Priya Life Science Egypt tracker

Sponsor

Fayoum University

Phase

Not applicable

Started

2025-08-01

Last updated

2025-07-23

Condition(s) studied

Alveolar Bone Loss

Investigational drug(s) / intervention(s)

subperiosteal tunneling for horizontal alveolar ridge augmentationconventional alveolar ridge augmentation

subperiosteal tunneling for horizontal alveolar ridge augmentation: subperiosteal dissection through horizontal incision only

conventional alveolar ridge augmentation: horizontal alveolar ridge augmentation through trapezoidal flap

Study summary

surgical horizontal augmentation for maxillary alveolar ridge using minimally invasive subperiosteal tunneling in comparison to conventional surgical technique

Eligibility

Sex

ALL

Min age

18 Years

Max age

60 Years

Healthy volunteers

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

Primary outcome measure(s)

Maxillary alveolar bone width — 6 months
increase of the alveolar bone buccolingually for horizontal ridge augmentation

Trial sites (1)

Facility	City	Region	Status
Fayoum University	Al Fayyum	Egypt

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07079917 on ClinicalTrials.gov ↗ ← All trials in Egypt