Tenting Screws Versus Autogenous Ring Block Grafts During Horizontal Ridge Augmentation

Not Applicable

• Conditions: Horizontal Ridge Deficiency

• Registration Number: NCT06845449
• Lead Sponsor: Fayoum University

Brief Summary

After administering local anesthesia,. A full-thickness mucoperiosteal flap will be incised and be reflected to expose the alveolar bone. The dimensions of the defect will be measured using a periodontal probe to determine the appropriate size of the block graft or the quantity of particle bone graft required.

In the non screw group, the blocks will be adapted to fit the recipient sites and secured to the alveolar bone using titanium bone fixation screws. Following the placement of the blocks, bovine particles will be applied over the graft and into any remaining gaps between the block and the recipient site, a resorbable collagen membrane (CM) will be shaped and placed over the graft and fixed using subperiosteal sutures.

In Tenting screw cases, the screws will be placed in suitable positions and depths, blocks will be crushed into particulates which will then be mixed with equal amount of bovine particles. the mixture will be applied to the recipient site all around the tenting screws a resorbable collagen membrane (CM) will be shaped and placed over the graft and fixed using subperiosteal sutures.

The flaps will then be sutured

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-02-20
• Study First Submitted QC: 2025-02-20
• Study First Posted: 2025-02-25
• Status Verified: 2025-03
• Study Start: 2025-03-10
• Last Update Submitted: 2025-03-21
• Last Update Posted: 2025-03-25
• Primary Completion: 2026-01-01
• Study Completion: 2026-02-27

Recruitment & Eligibility

• Status: ENROLLING_BY_INVITATION
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Patient has anterior maxillary horizontal defect less than 4mm in the alveolar ridge and (classified as class III or IV atrophy according to Cawood and Howell classification). (Cawood & Howell, 1988require horizontal bone augmentation in anterior maxilla before dental implant placement and in need of an implant-supported restoration in at least one site,
• Adult individuals aged 18 years or older
• Satisfactory oral hygiene,
• No previous history of bone augmentation procedures at the site to be treated in the study,
• The ability to comprehend and provide informed consent.

Exclusion Criteria

• Uncontrolled systemic disorders,
• Prior irradiation in the head and neck region,
• Immunosuppression or compromised immune system,
• Oral disorders such as lichen planus, ongoing or recent treatment with intravenous amino- bisphosphonates, untreated periodontitis,
• Poor oral hygiene and motivation,
• Parafunctional habits, pregnancy or lactation,
• Substance abuse involving drugs or alcohol, psychiatric disorders, a history (within the last 3 months) of regular use of smokeless chewing tobacco, smoking a pipe, cigar, or more than 10 cigarettes per day, acute or chronic infection or inflammation in the area, or
• Extraction with less than 3 months of healing.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Horizontal bone width gain	6months

Trial Locations

Locations (1)

Nahda University; 🇪🇬 Beni-seuf, Egypt

Nahda University

🇪🇬Beni-seuf, Egypt