CompletedNot Applicable

Clinical and Radiographic Evaluation of Topical Vitamin D on Immediate Dental Implants

Egypt24 participantsStarted 2022-10-11

Plain-language summary

This study evaluates the clinical and radiographic outcomes of topical vitamin D application on immediate dental implants in patients undergoing single-rooted tooth extraction in the anterior mandibular region.

Who can participate

Age range

21 Years – 40 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

. Both genders.
. Middle-aged adults (from 21 years to 40 years).
. Healthy American Society of Anesthesiologists patients (ASA I).
. Patients with teeth or roots indicated for extraction at the lower anterior region.

Exclusion criteria

. Pregnant or lactating females.
. Patients with parafunctional or bad oral habits such as bruxism or smoking (more than 10 cigarettes per day).
. Patients with bad oral hygiene.
. Patients with severe periodontal diseases (severe vertical or horizontal bone loss).
. Pathological changes or infections related to teeth indicated for immediate implant placement.

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 (ISQ)

Timeframe: Baseline, 3, and 6 months postoperatively

Bone Density

Timeframe: Baseline, 3 and 6 months postoperatively

Trial details

NCT IDNCT06806423

SponsorSuez Canal University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-01-01

View on ClinicalTrials.gov More Immediate Dental Implant trials