Maxillary Sinus Disease Clinical Trial
Official title:
Osteogenic Effects of Concentrated Growth Factors Applied in Maxillary Sinus Floor Elevation Via a Lateral Window Approach With Simultaneous Implant Placement: a Single-center Randomized Controlled Trial
Verified date | February 2017 |
Source | Deyang Stomatological Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To investigate the effects of concentrated growth factors applied in maxillary sinus floor elevation via a lateral window approach with simultaneous implant placement on repair of bone defects and new bone formation.
Status | Active, not recruiting |
Enrollment | 20 |
Est. completion date | May 2017 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Loss of one or more maxillary molars in the posterior maxillary region - Occlusogingival distance of > 4 mm - Residual bone height of 2-5 mm in the posterior maxillary region, no obvious maxillary sinus separation - No problems with the lungs, heart, or brain - Normal liver and kidney function - Normal coagulation function - Adequate prosthetic space - No history of bruxism or temporomandibular joint disorders - No tumors, cysts and polyps in maxillary sinus - No acute or chronic maxillary sinusitis - No acute periodontitis - No oral mucosal disease - Age 20-45 years - Able to tolerate the stress of anesthesia and surgery Exclusion Criteria: - Residual bone height of < 1 mm in the posterior maxillary region or presence of maxillary sinus mucosa rupture - Poor control of complex periodontal disease - Local inflammation or poor oral hygiene - Poorly treated maxillary disease - With severe bruxism - With temporomandibular joint disorders - Alcohol consumption and cigarette smoking (20 cigarettes/d) - Have a history of chemotherapy and radiation therapy in face and neck - Pregnant - With coagulation disorders - With autoimmune disease - With severe osteoporosis - With acute maxillary sinusitis - Unable to tolerate simple surgery because of systemic diseases including severe diabetes mellitus and heart disease - Unable to provide informed consent |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Deyang Stomatological Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Excellent and good rate of bone repair | X-ray examination was performed to evaluate bone repair as per excellent and good rate. | changes of month 1, month 3 and month 6 after surgery | |
Secondary | Bone density at bone defect sites | The thickness of the cortical bone at the defect sites was measured using a dental cone beam CT scanner to reflect bone density. | changes of month 1, month 3 and month 6 after surgery |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05494099 -
Extended Endoscopic Approaches to Non-malignant Maxillary Sinus Lesions Comparative
|
||
Completed |
NCT05596084 -
Comparison of the Use of Bovine Bone Graft and Titanium-Platelet Rich Fibrin in Maxillary Sinus Augmentation
|
N/A | |
Not yet recruiting |
NCT06071416 -
Biphasic Material With PRF in Lateral Sinus Floor Augmentation
|
Phase 1 | |
Not yet recruiting |
NCT04702867 -
Association Between Periodontal Bone Loss and Maxillary Sinus Changes.
|
||
Not yet recruiting |
NCT05411510 -
Evaluation of Bone Height Gain Following Trans-crestal Sinus Floor Elevation
|
N/A |