Actively Recruiting
Buccal Plate Augmentation Using Sticky Bone Versus Sticky Bone Filling in the Jumping Gap With Immediate Implant Placement in the Maxillary Esthetic Zone: A Randomized Controlled Trial
Led by Cairo University · Updated on 2024-10-23
20
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the pink esthetic score after Buccal Plate Augmentation using Sticky Bone compared to using Sticky Bone as a jumping gap filling material during immediate implant placement in the upper front teeth area. The study includes patients needing extraction of a non-restorable maxillary tooth in the esthetic zone, with intact buccal bone, to assess these two different surgical approaches. Patients will undergo clinical examinations including medical and dental history, periapical radiographs, and cone beam CT scans to evaluate bone and tooth root conditions before surgery. During treatment, venous blood will be collected to prepare platelet-rich fibrin (PRF) components mixed with bone particles to create sticky bone. In the experimental group, sticky bone is placed into a surgical pouch beside the buccal bone plate, while in the control group, sticky bone is used to fill the gap around the implant in the socket. Both groups receive immediate implant placement and healing abutment attachment. Participants will have follow-up visits at 3 and 6 months post-surgery for evaluation. Assessments include pink esthetic scoring, crestal bone level, thickness of the labial bone plate, soft tissue contour, and patient satisfaction. Standardized imaging and clinical exams will be used to monitor healing and implant integration. The total study duration includes these follow-ups to track outcomes and safety.
CONDITIONS
Brief Title
Buccal Plate Augmentation Using Sticky Bone With Simultaneous Immediate Implant Placement
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years or older
- Non-restorable maxillary tooth in the esthetic zone (front teeth and premolars) indicated for extraction
- Intact buccal bone plate after tooth extraction
- Full-mouth plaque and bleeding score not exceeding 20%
- Motivation to follow post-operative care and attend follow-up visits
You will not qualify if you...
- Periapical infection involving the tooth to be extracted
- Presence of periodontal disease
- Systemic health conditions affecting healing such as Diabetes Mellitus or Leukemia
- Pregnant or nursing females
- Smokers
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 - Single day procedure
Participants undergo atraumatic tooth extraction, immediate implant placement, and receive sticky bone grafting either in a surgical pouch for buccal plate augmentation or as a filling material in the jumping gap. Blood is drawn to prepare autologous PRF used in the grafting process, followed by placement of a healing abutment on the implant.
1 visit (in-person)
Duration - 6 months
Participants attend follow-up visits to assess healing, esthetic outcomes, crestal bone level, thickness of labial bone plate, soft tissue profile, and patient satisfaction up to 6 months after the implant placement.
Visits at immediately after implant placement, 3 months, and 6 months postoperatively
Trial Site Locations
Total: 1 location
1
Faculty of Dentistry Cairo University
Cairo, Egypt, 12613
Actively Recruiting
Research Team
Y
Yara KH Ghaith
E
Enji ahmed, Professor
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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