Outcomes of Different Bone Graft Combinations for Maxillary Sinus Augmentation Procedure (NCT07512011) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Outcomes of Different Bone Graft Combinations for Maxillary Sinus Augmentation Procedure
United States10 participantsStarted 2026-06
Plain-language summary
This study investigates the outcomes of a surgical procedure that is performed to increase bone support at a future implant site on the upper back jaw area. This procedure requires placing bone graft material and/or substitutes into the maxillary sinus. The average healing time for the graft is about 6 months. Then, the site will be ready for dental implant. The study will compare healing outcomes of two types of bone graft mixtures used on the same patient (right and left upper jaw regions). The outcomes will be evaluated through clinical examination but also by studying the quality of the tissue through tissue biopsies obtained from grafted sites.
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Indication of bilateral sinus augmentation through lateral window technique to prepare maxillary right and left posterior edentulous sites for a single or multiple unit implant supported restorations.
* Systemically healthy with controlled conditions
* Periodontally healthy/controlled dentition
* No known chronic and/or seasonal sinusitis
* No previous ear, nose, throat, and sinus surgeries
* Non-smokers
* Willing to be treated with allograft, xenograft and/or synthetic bone graft materials
Exclusion Criteria:
* 1\. Indication of sinus augmentation through indirect techniques (≥5 mm initial alveolar ridge height from crest to maxillary sinus floor)
* Implant placement surgery planned somewhere else
* Implant placement planned at the time of sinus augmentation
* Cases requiring major alveolar ridge augmentation concurrent with sinus augmentation
* Cases requiring the use of a partial denture with buccal flange extension during the post-operative period
* History of previously failed implant and/sinus augmentation procedures
* History of tumors and/or radiation and/or chemotherapy
* Uncontrolled systemic health problems and ENT/sinus concerns
* Uncontrolled periodontal/dental problems
* Intake of medications affecting wound or bone healing (e.g., corticosteroids, immunosuppressants, etc.)
* Alcohol or drug abuse
* Active smokers (patient should be a non-smoker for at least 1 year prior to sinus augmentation procedure)
* Unable/unwilling to follow post-o…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in ridge dimensions
Timeframe: Prior to procedure; 10 days post-procedure; 1 month post-procedure; 6 months post-procedure
2
Change in Bone Density
Timeframe: Prior to the procedure; 4 months post-procedure