CompletedNot Applicable

Different Drilling Techniques in Posterior Maxilla

Egypt32 participantsStarted 2025-05-01

Plain-language summary

The study aimed to evaluate clinically and radiographically the effect of Magnetic Mallet technique versus Conventional Drilling technique on early loaded implant in posterior maxilla.

Who can participate

Age range

18 Years – 50 Years

Sex

FEMALE

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: * Patient with missing one or more posterior maxillary teeth. * Patients in the age group between 18 and 50 years old. * 10 mm or more vertical bone height is present. * No gender preface in selection of the patients. * Good oral hygiene. * Non-smokers. * Patients willing to be present during the study follow up intervals. * Patients free from any systemic diseases. * 6 mm or more ridge width is present. * Crown height space of at least 8 mm. •!Patients without any para-functional habits (bruxism and clenching). Exclusion Criteria: * Patients with any pathological lesion or root tips at the planned surgical site. * Patients with systemic diseases that contra-indicate the surgical procedure or affect bone healing process such as uncontrolled diabetes mellitus, bleeding disorders. * serious osseous disorders, and mental disorders. * Patient taking drugs that could affect bone healing process as in * Immunosuppressive drugs and bisphosphonates. * Alcoholism. * Untreated periodontal disease or bad oral hygiene. * Pregnancy.

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

Implant stability

Timeframe: 9 months

Bone Density measurement

Timeframe: 9 months

Marginal Bone Loss (MBL)

Timeframe: 9 months

Trial details

NCT IDNCT07606456

SponsorMansoura University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-05-01

View on ClinicalTrials.gov More Implant Dentistry trials

Who can participate

Age range

18 Years – 50 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.