Comparison of open Sinus Lift by Piezosurgery and Conventional Rotative Instruments
Phase 3
- Conditions
- bone deficiency in the posterior maxillary region.
- Registration Number
- IRCT20150504022085N2
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Age over 18 years
At least 4 months after tooth loss
requiring dental implant in the posterior maxillary region (residual alveolar bone height,5 mm or less bilateral)
Signature of consent form
Exclusion Criteria
History of Bone Metabolic Diseases
smoking
Contraindications for implant placement
Immune system defects
Infection in maxillary region
Sinusitis
Endocarditis
Sensitivity to penicillin and its derivatives
Destructive parafunctional habits
requiring Advanced Bone Surgery or Ridge Augmentation
Pregnancy and lactation
Uncontrolled diabetes
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: 2 and 7 days after surgery. Method of measurement: with Visual analogue scale.;Edema. Timepoint: 2 and 7 days after surgery. Method of measurement: with Visual analogue scale based on Pasqualini et al. (2005).;Duration of surgery. Timepoint: From the beginning of the osteotomy to the end of the bone window preparation. Method of measurement: Stopwatch.
- Secondary Outcome Measures
Name Time Method