Assessment of Osseointegration Properties of Nano-Hydroxy Apatite Coated Titanium Implant (NCT05936775) | Clinical Trial Compass
CompletedNot Applicable
Assessment of Osseointegration Properties of Nano-Hydroxy Apatite Coated Titanium Implant
Egypt30 participantsStarted 2023-06-22
Plain-language summary
the purpose of this trial is to evaluate the osseointegration properties of nano-hydroxy apatite coated titanium implants in posterior maxilla. 30 patients will be included in this trial divided into two groups, control and intervention. Primary and secondary implant stability will be measured
Who can participate
Age range
18 Years – 49 Years
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
. Patients with missing at least one maxillary posterior tooth
. Patients free from any systemic disease
. Patients who approve to be included in the trial and sign the informed consent
. Patients with no intra-bony defect.
. Adults aged 18 years old and above
Exclusion criteria
. Patients who are allergic to titanium
. Heavy smoker patient
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
Implant stability
Timeframe: immediately post-operative
2
Implant stability
Timeframe: 4 weeks post-operative
3
Implant stability
Timeframe: 6 weeks post-operative
4
Implant stability
Timeframe: 12 weeks post-operative
Trial details
NCT IDNCT05936775
SponsorOctober University for Modern Sciences and Arts