Preimplant Site Augmentation Using MPM Versus Autogenous Bone Graft
Not Applicable
- Conditions
- Bone Resorption
- Registration Number
- NCT03007069
- Lead Sponsor
- Cairo University
- Brief Summary
Using growth factors obtained from patient's venous blood mixed with particulate autogenous bone the study compares bone gain by implant with gold standards.
- Detailed Description
To study the effectiveness of MPM in ridge augmentation with implant insertion compared with autogenous bone graft.
-PICO-
Population (P): Patients with defective maxillary alveolar ridge requiring implant insertion.
Intervention (I): Ridge augmentation with MPM.
Comparator (C): Autogenous bone graft.
Outcome (O): Patient satisfaction - Implant stability.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- Medically free patients.
- Evaluated bone height on CBCT to be (0-4 mm buccal bone dehiscence) and width (not less than 4.5 mm)
- Patients with Anterior maxillary defective partially edentulous ridge.
- Age between 18 and 40 years.
- Both sexes.
- Patients physically able to tolerate surgical and restorative procedures.
- Patients with an opposing tooth to the pre-implant site.
- Good oral hygiene.
- Highly motivated patients.
Exclusion Criteria
- Patients allergic to local anesthetic agent.
- Pregnant or lactating females.
- Presence of any pathosis in the pre-implant site.
- Presence of any mucosal disease.
- Presence of parafunctional habits.
- History of oral radiotherapy.
- History of prolonged steroids use.
- Psychological disorders.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Patient Satisfaction regarding esthetic results , outcome will be measure using questionnaire. 5 months
- Secondary Outcome Measures
Name Time Method Stability of dental implants , this will be measured using Ostell device in ISQ units. 5 months.