- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03626779
Bone Density in Immediate Implant Placment and Loading(BDIIPL)
August 21, 2018 updated by: Ahmed adel shaaban
Prf Controlled,Randamized Cinical Trial of EFFECTS OF THE PLATELET-RICH FIBRIN (PRF) ON BONE DENSITY IN IMMEDIATE IMPLANT PLACEMENT AND LOADING IN ESTHETIC ZONE
Atrumatic extraction ,immediate implant placment , prf as plug,immediate loading , mesure bone density 0-3-6-9 month
Study Overview
Detailed Description
Atrumatic extraction unrestorable tooth in esthetic zone and immediate implant placment and withdrow 10cc blood sample to gain prf plug as membrane and immediate provisional for one week and final restoration after 1 week , and mesure bone density from 0-3-6-9 month
Study Type
Interventional
Enrollment (Anticipated)
10
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion criteria:
- unrestorable anterior tooth.
- Good oral hygine
- Adequate bone hieght apical to the alveolus of failing tooth to ensure primary stability .
Exclusion Criteria:
- systematic disease which affect osteointgration.
- 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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: immediate placment and loading with prf
Immediat placment and loading with prf
|
Take 10cc blood from patient and gain prf blug
|
No Intervention: immediate implant placment and loading
Immediate implant placment and loading without prf
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Bone density enhancement with prf in immediate implant placment and loding
Time Frame: 9 month
|
Cbct
|
9 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
September 1, 2018
Primary Completion (Anticipated)
August 30, 2019
Study Completion (Anticipated)
August 30, 2019
Study Registration Dates
First Submitted
July 30, 2018
First Submitted That Met QC Criteria
August 9, 2018
First Posted (Actual)
August 13, 2018
Study Record Updates
Last Update Posted (Actual)
August 22, 2018
Last Update Submitted That Met QC Criteria
August 21, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Cairo U
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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