Actively Recruiting
Labial Bone Thickness Change in Immediate Implant Placement In Maxillary Esthetic Zone
Led by Cairo University · Updated on 2026-04-03
22
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to assess the effect of distance between the implant and the bone on the resultant bone thickness adjacent to the implant in place of a broken down tooth that happens to be bounded by two natural teeth. The main questions it aims to answer are: Does the horizontal implant position (and hence the gap between the implant and the socket wall i.e. jumping gap) affect the resultant labial bone thickness? Will it affect the quality of soft tissue, esthetics and patient satisfaction? Participants will have an implant placed using a surgical guide with a jumping gap either less than 2 mm or equal or more than 2 mm and will be asked to visit the clinic once every 3 months for checkups, radiographs, and readings.
CONDITIONS
Official Title
Labial Bone Thickness Change in Immediate Implant Placement In Maxillary Esthetic Zone
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with a single non-restorable upper front tooth (FDI 15-25)
- Age between 21 and 65 years old
- Good oral hygiene with bleeding on probing less than or equal to 10%
- Willing and able to follow study visits for one year
- Remaining labial bone thickness of at least 1 mm confirmed by CBCT and during surgery
You will not qualify if you...
- Active infection related to the tooth to be replaced
- Presence of labial bone defects such as fenestration or dehiscence
- Large cyst or pathological lesion near the tooth
- History of radiation therapy to the upper jaw
- History of bisphosphonate or anti-resorptive drug use
- Uncontrolled systemic or metabolic diseases
- Parafunctional habits or active gum disease
- Smoking more than 10 cigarettes per day
- Alcohol abuse
AI-Screening
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Trial Site Locations
Total: 1 location
1
Cairo University
Cairo, Egypt
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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