Clinical comparison of sinus lift via piezosurgery and usual rotary techniques
Not Applicable
- Conditions
- Sinus lift surgery.
- Registration Number
- IRCT20221209056759N1
- Lead Sponsor
- Sanandaj University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 22
Inclusion Criteria
Over 18 years old
Needing bilateral sinus lift and implant for the posterior areas of maxilla
Systematically healthy
Exclusion Criteria
Immune system defect
Infection in poterior areas of maxilla
Sinusitis
Needing advanced bone surgery or transverse ridge augmentation
Destructive parafunctional habit
Pregnant or lactating women
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 24, 48, 72 hours and 1 week after surgery. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Sinus perforation. Timepoint: During the surgery. Method of measurement: Surgeon's observation.;Time of surgery. Timepoint: During surgery. Method of measurement: Minures.;Field of view of the surgery. Timepoint: During the surgery. Method of measurement: Four point scale.;Eating and sleeping. Timepoint: During the week after surgery. Method of measurement: Pittsburgh Sleep Quality Index and a valid questionnaire for Eating changes.