Actively Recruiting
Assessment of Dental Implants Placed in Mandibular Consolidated Iliac-Crest Bone Grafts Using Densah Burs Versus Standard Drills A Randomized Controlled Trial
Led by Beni-Suef University · Updated on 2024-06-27
12
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This trial studies patients who have undergone mandibular bone grafts from the iliac crest, a common source of bone for dental implants. Researchers are evaluating whether using a bone-condensing technique called osseodensification with densah burs can improve the stability of dental implants and reduce bone loss around the implant compared to conventional bone drilling. The study is randomized and double-blinded to compare these two drilling approaches. Participants will be divided into two groups: one group will have dental implants placed using the osseodensification technique with densah burs, and the other group will have implants placed with standard bone drills. This study focuses on implants placed in consolidated mandibular bone grafts following segmental mandibular resection. The observation period for implant stability and bone loss is six months after implant placement. Participants will be evaluated over a six-month osseointegration period during which radiographic images will be taken to measure bone loss around the implants. Implant stability will also be assessed during this time. The study will monitor the bone and implant condition closely, aiming to understand the differences between the two drilling techniques in supporting implant success. The total age range for participants is 18 to 55 years, and healthy soft tissue coverage around the implant site is required.
CONDITIONS
Brief Title
Assessment of Implants Placed in Consolidated Graft With Different Bone Drills.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients of both sexes aged 18 to 55 years
- Patients who had a successful iliac crest mandibular bone graft after segmental mandibular resection
- Jaw ridge with at least 10 millimeters height and 7 millimeters width
- Healthy soft tissue coverage with reasonable interaction space
You will not qualify if you...
- Signs of graft infection, rejection, or major resorption
- Previous exposure to radiotherapy or chemotherapy
- Any systemic disease affecting bone healing or implant integration
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 months osseointegration period
Participants receive dental implants placed in consolidated mandibular bone grafts using either densah burs or standard drills.
1 baseline visit and periodic follow-up visits during the 6 months
Trial Site Locations
Total: 1 location
1
Department of Oral and Maxillofacial Surgery, Faculty of Oral and Dental Medicine, Modern University for Technology & Information.
Cairo, Egypt
Actively Recruiting
Research Team
M
Maged Seleet, PHD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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