Clinical Trials Directory

Trials / Completed

CompletedNCT07060027

Single vs. Double Tenting Screws for Horizontal Ridge Augmentation.

The Effect Of Single Versus Double Screws In Tenting Screw Technique For Horizontal Ridge Augmentation Before Dental Implant Placement (Randomized Clinical Trial)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Omar Saad · Academic / Other
Sex
All
Age
20 Years – 55 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to learn if using two screws works better than one screw for building up jawbone width before dental implant placement. It will also check the safety of both techniques. The main questions it aims to answer are: * Does using two screws give better bone growth than using one screw? * Which technique creates more stable bone for dental implants? Researchers will compare the single-screw technique to the double-screw technique to see which works better for jawbone reconstruction. Participants will: * Receive either one or two small titanium screws placed in their jawbone to support a bone graft * Have the graft covered with a protective membrane * Return after 6 months for screw removal and dental implant placement * Attend follow-up visits to check healing progress The study will help dentists determine the best method for patients who need jawbone reconstruction before getting dental implants. All procedures use FDA-approved materials and follow standard surgical protocols. New chat

Conditions

Interventions

TypeNameDescription
PROCEDUREhorizontal bone augmentation using single tenting screwPatients in this group will undergo guided bone regeneration (GBR) using a single titanium bone screw placed in the crestal position to stabilize the graft material. The surgical procedure includes sulcular and vertical releasing incisions, elevation of full-thickness buccal and palatal/lingual flaps, and multiple cortical perforations to enhance angiogenesis. The defect will be filled with particulate allograft extended 10-12 mm apicocoronally and covered with a bovine pericardium membrane. A tension-free primary closure will be achieved using 5-0 polypropylene sutures. Bone screw removal and implant placement will occur 6 months postoperatively. This group is distinguished by the use of a single crestal screw for graft stabilization compared to dual-screw fixation in the control group.
PROCEDUREhorizontal bone augmentation using Double tenting screwParticipants in this group will receive guided bone regeneration (GBR) with two titanium bone screws for enhanced graft stabilization. One screw will be placed at the crestal level, while a second screw will be inserted 5 mm apical to the first, providing vertical stabilization of the graft material. The procedure involves sulcular and vertical releasing incisions, full-thickness flap elevation on both buccal and palatal/lingual aspects, and multiple cortical perforations to stimulate vascularization. The defect will be filled with particulate allograft extending 10-12 mm apicocoronally and covered with a bovine pericardium membrane. Tension-free primary closure will be performed using 5-0 polypropylene sutures. At 6 months, screws will be removed and dental implants placed. This intervention is distinguished by the dual-screw fixation technique, designed to provide greater mechanical stability compared to the single-screw approach used in the comparator group.

Timeline

Start date
2022-08-01
Primary completion
2024-01-25
Completion
2024-12-10
First posted
2025-07-11
Last updated
2025-07-11

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07060027. Inclusion in this directory is not an endorsement.