Comparing implant stability in post-extraction sockets
Official title: Effect of Time and Local Factors on Hydrophilic Tissue Level Implants in Post-extraction Sites: a RCT
Run by University of Rome Tor Vergata · NCT06711744 · Data updated 2026-11-12
This study is testing how two different types of dental implants affect healing and stability in patients who have just had a tooth removed.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 99 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | University of Rome Tor Vergata Academic / other |
| Locations | 1 site (Rome, RM) |
| Status | Recruiting |
| Started | January 31, 2025 |
| Main results expected | December 31, 2026 |
| Study ends | February 28, 2027 |
| Registry record updated | March 28, 2025 |
| Trial ID | NCT06711744 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults over 18 with failing teeth who have intact extraction sockets and no significant periodontal issues.
✕Probably not a fit
Patients with systemic diseases like diabetes or osteoporosis, or those who smoke heavily, may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the differences in implant stability quotient (ISQ) between two different types of dental implants placed in post-extraction sockets. Patients aged 18 and older with failing teeth will have their implants monitored monthly for ISQ from the moment of insertion up to 12 months. The goal is to determine how the macro design of the implants affects bone healing and stability. The study focuses on patients with intact socket walls following atraumatic tooth extractions.
Why it matters
Potential benefit: If successful, this study could lead to improved dental implant outcomes and better bone healing for patients receiving implants.
How similar studies have gone: While there have been studies on implant stability, this specific comparison of macro design in post-extraction sockets is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients (at least 18 years old) presenting with failing tooth. * no recession of gingival contour of tooth to be extracted * no periodontal bone loss of neighboring teeth * no implants in neighboring teeth * class I extraction socket (intact buccal wall) * atraumatic extraction of the tooth with intact socket walls remaining. Exclusion Criteria: * deep bite (severe II class) * systemic disease (diabetes, osteoporosis) * heavy smokers (more than 10 cigarettes/day)
Where it's running
-
Paolo Carosi
Rome, Rm, Italy Recruiting
Study contacts
- Study coordinator: Paolo Carosi, PhD
- Email: paolo.carosi@alumni.uniroma2.eu
- Phone: +393277998699
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.