Autologous Demineralized Dentin Graft With or Without Melatonin for Immediate Implant Osseointegr… (NCT07610876) | Clinical Trial Compass
RecruitingNot Applicable
Autologous Demineralized Dentin Graft With or Without Melatonin for Immediate Implant Osseointegration
Egypt16 participantsStarted 2025-08-11
Plain-language summary
This randomized clinical study aims to evaluate the effect of autologous demineralized dentin graft (ADDG) with or without melatonin gel on the osseointegration of immediately placed dental implants in the maxillary premolar region. Sixteen patients requiring extraction and immediate implant placement will be randomly allocated into two groups. Clinical and radiographic outcomes including implant stability, peri-implant probing depth, modified bleeding index, marginal bone loss, buccal bone thickness, and bone density will be evaluated over a 9-month follow-up period.
Who can participate
Age range
20 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:
* Age above 20 years
* Non-restorable maxillary premolar teeth
* Candidates for immediate implant placement
* Intact socket walls
* Jumping gap \>2 mm
* Non-smokers or light smokers
* No acute infection
* Adequate bone for primary stability
Exclusion Criteria:
* Heavy smokers
* Bruxism or clenching
* Uncontrolled systemic disease
* Chemotherapy/radiotherapy
* Immunocompromised patients
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 Quotient (ISQ)
Timeframe: Baseline and 6 months
2
Jumping Distance
Timeframe: Immediate postoperative and 9 months after implant placement
3
Marginal Bone Loss
Timeframe: Immediate postoperative and 9 months after implant placement
4
Bone Density
Timeframe: Immediate postoperative and 9 months after implant placement