A Study of Surgical Guide Assisted Dental Implantation in Bangladesh (NCT05983718) | Clinical Trial Compass
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A Study of Surgical Guide Assisted Dental Implantation in Bangladesh
Bangladesh28 participantsStarted 2023-08-23
Plain-language summary
This is a randomized controlled study that aims to compare the accuracy between full-guided with guide-pin-assisted free-hand dental implant surgeries. The basis of evaluation in each case is the comparison of the preoperative digital plan with the actual postoperative status.
Who can participate
Age range
18 Years – 75 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 of age between 18 to 75 and of any gender
* Patient fit for implantation (satisfactory soft and hard tissue conditions and occlusion)
* Partially edentulous patient
Exclusion Criteria:
* Patient with pregnancy
* Patient with uncontrolled diabetes mellitus.
* Patient who needed dentoalveolar or associated soft tissue reconstruction procedure
* Patient taking bisphosphonate or have any history of systemic or local bone disease
* Recent extracted sites
* Patients with a history of smoking, alcoholism
* Patient with a history of head-neck radiation
* Patient with associated periapical pathology or history of parafunctional habit
* Patient needs bone grafting.
* Known HIV, Hepatitis B, or Hepatitis C infection.
* Limited mouth opening, which, in the examiner's opinion, would risk the success of the intervention
* Local infection
* Known allergy to any component of the implant or the implant guide
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.