Clinical trial Recruiting at 1 site Observational Ages 18 to 90

Probing around dental implants before versus after crown removal to detect peri-implantitis

Official title: The Study on the Accuracy of Peri-implant Probing and Related Influencing Factors

Run by The Dental Hospital of Zhejiang University School of Medicine · NCT07004517 · Data updated 2026-11-12

This test will see if measuring pocket depth and bleeding around dental implants before versus after taking off the crown finds peri-implantitis more accurately in adults with restored implants.

Quick facts

Study typeObservational
Ages18 Years to 90 Years
SexAll
Enrollment83 (estimated)
SponsorThe Dental Hospital of Zhejiang University School of Medicine
Academic / other
Locations1 site (Hangzhou, Zhejiang)
StatusRecruiting
StartedJanuary 11, 2024
Main results expectedJune 2025
Study endsAugust 2025
Registry record updatedJune 4, 2025
Trial IDNCT07004517 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults over 18 whose implants are osseointegrated with a final restoration in place for at least one month and who need the restoration removed for any reason.

Probably not a fit

Patients who cannot have the prosthesis completely removed, those with serious systemic disease, severe intraoral infection, recent crown removal/re-restoration within one month, pregnancy/lactation, or who refuse participation may not receive 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 is a diagnostic accuracy study comparing peri-implant probing depth (PPD) and bleeding on probing measured before prosthesis removal (PPD-1) and after crown removal (PPD-2). Investigators will record probing depths and bleeding, document prosthetic design features, and compare how well pre- and post-removal measurements identify peri-implantitis. The study will analyze factors that influence probing accuracy, such as prosthesis shape and access. It is a single-center observational study conducted at a dental hospital in Hangzhou, China.

Why it matters

Potential benefit: If successful, the results could help clinicians decide whether removing a prosthesis before probing improves diagnosis and leads to earlier, more accurate treatment of peri-implantitis.

How similar studies have gone: Some prior research has examined peri-implant probing and bleeding on probing, but direct diagnostic comparisons of measurements before versus after crown removal are limited, so this approach is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age greater than 18 years.
2. The implant has completed osseointegration and has undergone final restoration for at least one month.
3. The final restoration needs to be removed or retrieved for various reasons.

Exclusion Criteria:

* Patients with serious systemic diseases, severe intraoral infections, severe mental disorders, pregnancy/lactation in women, or other conditions that make oral treatment operations unsuitable.
* History of crown removal or re-restoration within the past month prior to the visit.
* The prosthesis has fallen off or is severely damaged and has lost its original form before the visit.
* The prosthesis cannot be completely removed.
* Refusal to participate in this study.

Where it's running

  • The Affiliated Stomatology Hospital of Zhejiang University School of Medicine
    Hangzhou, Zhejiang, China
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.