Clinical Outcomes of Immediate Implants With or Without a Volume-stable Collagen Matrix (NCT05081284) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Clinical Outcomes of Immediate Implants With or Without a Volume-stable Collagen Matrix
Italy40 participantsStarted 2022-01-10
Plain-language summary
The purpose of this study is to evaluate the soft tissue clinical results in patients that received, or not, a soft tissue augmentation around dental implant inserted immediately after the extraction.
Who can participate
Age range
18 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:
\- Presence of a single failing tooth in the esthetic region (second premolar to contralateral second premolar), the adjacent teeth should be present and without any dental pathologies.
Exclusion Criteria:
* Patients who are heavy smokers (more than 10 cigarettes/day);
* Patients who suffer from any systemic diseases that could negatively influence wound healing;
* Patients who received head and neck radiation treatment;
* Patients who have a full contraindication to implant surgery;
* Patients who have uncontrolled periodontal disease;
* Patients who show a full mouth plaque and bleeding score higher than 25%;
* Patients who have deficient extraction sockets according to the classification of Juodzbalys et al. 2008.
* Patients with known allergy, sensitivity or intolerance to collagen
* Patients who are pregnant or who are breastfeeding
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.