Influence of Provisional Restoration Type on Outcomes of Immediate Implant Placement and Loading (NCT07700771) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Influence of Provisional Restoration Type on Outcomes of Immediate Implant Placement and Loading
Egypt60 participantsStarted 2025-12-01
Plain-language summary
A randomized clinical trial comparing 3D-printed resin and CAD/CAM-milled PMMA provisional restorations used for immediate loading of fully digitally guided immediate implants.
Who can participate
Age range
18 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 presenting with non-restorable teeth in the maxillary esthetic zone indicated for extraction and immediate implant placement.
* Age ranging from 18 to 50 years.
* Adequate interarch relationship and interocclusal space to accommodate the planned prosthetic restoration.
* Intact extraction socket walls with a jumping gap not exceeding 4 mm, as measured on preoperative CBCT images. The jumping gap will be defined as the horizontal distance between the implant surface and the inner aspect of the buccal socket wall and will be grafted in all cases.
* Good oral hygiene and periodontal health.
* Willingness to attend all follow-up visits and comply with study requirements.
Exclusion Criteria:
* Presence of acute infection, pathological lesions, or severe periodontal disease at the planned implant site.
* Smokers.
* Alcohol or drug abuse.
* Patients with systemic conditions contraindicating implant surgery (e.g., uncontrolled diabetes mellitus, bleeding disorders, immunosuppression, recent radiotherapy to the head and neck region).
* Pregnancy or lactation.
* Patients with parafunctional habits such as bruxism or clenching.
* Inability to maintain adequate oral hygiene or attend follow-up visits.
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
Peri-implant soft tissue changes
Timeframe: Baseline (immediately after provisionalization), 1 month, 3 months, and 6 months postoperatively.