Bone Density in Immediate Implant Placment and Loading(BDIIPL)
NCT ID: NCT03626779
Last Updated: 2018-08-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
10 participants
INTERVENTIONAL
2018-09-01
2019-08-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Osseodensification Plus Platelet Rich Fibrin With Simultaneous Implant Installation in Closed Sinus Lift
NCT05797675
Efficacy of Different Osseodensification Techniques
NCT07061015
Assessment of Bone Density in Impacted Mandibular Third Molar
NCT05944939
Demineralized Whole-tooth vs Demineralized Particulate Dentin Grafts in Alveolar Ridge Preservation
NCT05336149
Effect of Local Application of Simvastatin Versus Bone Powder on Implant Bone Changes
NCT06016218
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
immediate placment and loading with prf
Immediat placment and loading with prf
Prf
Take 10cc blood from patient and gain prf blug
immediate implant placment and loading
Immediate implant placment and loading without prf
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Prf
Take 10cc blood from patient and gain prf blug
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Good oral hygine
* Adequate bone hieght apical to the alveolus of failing tooth to ensure primary stability .
Exclusion Criteria
* Bad oral hygiene
* Broxism, clenching, deep bite, edge to edge and abnormal habits.
* Non-treated peeiodontal diseases.
* Pregnancy and smokers. Severe infection. Loss of labial crest after extraction of failing tooth.
20 Years
45 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ahmed adel shaaban
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ahmed adel shaaban
CairoU
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Cairo U
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.