Low-Level Diode Laser Therapy on the Acceleration of Osseointegration Around Delayed Dental Implant (NCT07536451) | Clinical Trial Compass
CompletedNot Applicable
Low-Level Diode Laser Therapy on the Acceleration of Osseointegration Around Delayed Dental Implant
Egypt20 participantsStarted 2024-06-01
Plain-language summary
Good quality soft tissue determines the possibility not only to obtain full primary wound closure during the bone defect reconstruction, but also assures effective implant treatment and stability of peri-implant condition.Moreover, it is very important to assure the proper emergence profile of the implant supported restorations, which give the opportunity to achieve the highest aesthetic appearance. In the long-term, the correct width and thickness of the attached keratinized tissue is the key point to ensure the stable position of the mucosal line around the implant's neck. The promising outcomes of laser on soft and hard tissue have been demonstrating in a variety of studies. Therefore, the aim of this clinical study is to evaluate the efficacy of LLDLT on enhancing osseointegration and on the peri-implant mucosal tissue around delayed dental implants.
Who can participate
Age range
20 Years – 50 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 are systemically medically free.
* Ability to maintain good oral hygiene as evidenced in recall visits.
* Sufficient mesiodistal and interocclusal space and have an intact buccal bone contours which does not require bone augmentation procedures.
* Adequate bone quality.
* Keratinized tissue ≥ 2mm.
* Thickness of the gingiva ≥ 1 mm.
Exclusion Criteria:
* Presence of any systemic disease that could influence the outcome of the therapy.
* Presence of any risk factor e.g.; smoker, pregnant, lactating patients or any disease affect bone healing.
* Previous history of periodontal surgical treatment in quadrant selected for the study.
* Restorations or caries in the area to be treated and non-vital tooth.
* Adjacent teeth are tilted or rotated.
* Patients taking medications known to cause affect bone quality.
* Traumatic occlusion or Para-functional habits such as clenching or bruxism.
* Participation in other clinical trials.
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 marginal bone loss
Timeframe: 2 weeks, 1month, 2 months, and 6 months
2
Change in in implant stability
Timeframe: Immediately after surgery, 2 months and 6months postoperative.