Evaluation the Accuracy of Immediate Implant Placement Using SocketFit Static Surgical Guide Vers… (NCT07760974) | Clinical Trial Compass
RecruitingNot Applicable
Evaluation the Accuracy of Immediate Implant Placement Using SocketFit Static Surgical Guide Versus Conventional Static Surgical Guide in Anterior Esthetic Zone
Egypt26 participantsStarted 2026-08-01
Plain-language summary
This study compares two types of surgical guides used during immediate dental implant placement in the upper front teeth. One guide is a conventional static surgical guide, while the other is a modified SocketFit static surgical guide designed to improve stability after tooth extraction. The purpose of the study is to determine whether the SocketFit guide improves the accuracy of implant placement.The findings may help improve the precision and predictability of immediate dental implant treatment in the anterior esthetic zone.
Who can participate
Age range
18 Years – 35 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 in good health with absence of any relevant medical condition that contraindicates dental implant placement e.g. blood coagulation disorder.
* Optimal compliance is evidenced by no missed treatment appointments and a positive attitude toward oral hygiene.
* Extraction socket type I according to Ellian et al criteria with adequate native/apical bone to achieve primary implant stability and intact buccal plate of bone.
* Thick mucosal phenotype.
* Probing depth ≤ 3 mm at mid-buccal aspect of failing tooth.
* Age ranged from 18- 35 years old of both genders.
Exclusion Criteria:
* Patients subjected to irradiation in the head and neck area.
* Bisphosphonate therapy.
* Females who are pregnant or trying to conceive, and nursing mothers.
* Smokers and uncontrolled diabetic 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
Coronal deviation
Timeframe: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
2
apical deviation
Timeframe: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
3
depth(vertical) deviation
Timeframe: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
4
angular deviation
Timeframe: Immediately after implant placement following digital superimposition of the planned and actual implant positions.