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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 December 2017 |
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Main ID: |
NCT03049137 |
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Date of registration:
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06/02/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Computer Guided Versus Conventional Augmentation Using Bone Ring
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Scientific title:
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Evaluation of Computer-Guided Versus Conventional Simultaneous Implant Placement With Ridge Augmentation Using an Autogenous Bone Ring Graft With PRF on Patient's Esthetic Satisfaction |
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Date of first enrolment:
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February 2017 |
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Target sample size:
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10 |
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Recruitment status: |
Not yet recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03049137 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Egypt
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Contacts
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Name:
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Mohamed A Younis, Dentist |
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Address:
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Telephone:
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01156674425 |
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Email:
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younismatador@gmail.com |
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Affiliation:
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Name:
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mohamed A Younis, Dentist |
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Address:
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Telephone:
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Email:
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Patients with insufficient alveolar ridge or severe alveolar bone resorption
horizontally and vertically in partially edentulous maxillary anterior region.
2. Medically free patients in order to be a confounding factor on the final results.
3. Highly motivated patients.
4. Good oral hygiene.
5. Patients physically able to tolerate surgical and restorative procedures.
Exclusion Criteria:
1. Young patients (incomplete bone growth).
2. Patients with any systemic disease that could affect bone healing.
3. Patients allergic to local anaesthetic agent.
4. Pregnant or lactating females.
5. Presence of any pathosis in the area.
6. history of oral radiotherapy.
7. history of prolonged steroid use.
8. Psychological disorders.
Age minimum:
21 Years
Age maximum:
55 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Bone Resorption
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Intervention(s)
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Device: implant
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Procedure: Computer Guided Stent Augmentation
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Drug: Platelet-rich fibrin (PRF)
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Procedure: Free Hand Augmentation
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Primary Outcome(s)
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Patient Satisfaction regarding esthetic results.
[Time Frame: 5 month]
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Secondary Outcome(s)
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Accuracy of computer guided surgical templates in comparison with 3D virtual planning.
[Time Frame: immediately after procedure]
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Secondary ID(s)
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CairoBRG-PRF
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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