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Effect of Probe Material (Metallic vs. Plastic) on Peri-implant Probing: a Randomized Clinical Trial.

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Evaluate whether the type of probe (plastic vs. metallic) modifies the accuracy of peri-implant probing in single-unit implants, by comparing the probing depth recorded with the prosthesis in place versus without the prosthesis (ΔPD, mm). Secondarily, explore the influence of prosthetic design and implant position on probing values and on other clinical and radiographic parameters.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults (≥18 years)

• Presence of at least one single-unit bone-level implant rehabilitated with a screw-retained prosthesis directly connected to the implant (no intermediate abutment)

• Implant in function for at least 1 year after prosthetic loading

• No pathological bone loss on periapical radiograph (distance from the most coronal rough surface of the implant to the bone crest \< 3 mm)

• Ability to understand and sign informed consent

• Peri-implant health or mucositis, defined according to the 2017 World Workshop criteria:

• Health: no clinical signs of inflammation, lack of profuse (line or drop) bleeding on probing, no increase in probing depth compared to previous records, and no progressive bone loss beyond initial remodeling (\<2 mm). In the absence of previous radiographs, radiographic bone level \<3 mm without bleeding and/or suppuration on probing.

• Mucositis: presence of bleeding and/or suppuration on probing, no increase in probing depth compared to previous records, and no bone loss beyond initial remodeling (\<2 mm). In the absence of previous radiographs, radiographic bone level \<3 mm with bleeding and/or suppuration on probing.

Locations
Other Locations
Spain
Hospital Odontològic Universitat de Barcelona
RECRUITING
L'hospitalet De Llobregat
Contact Information
Primary
Octavi Camps Font, DDS MS PhD
ocamps@ub.edu
+34 934 024 269
Time Frame
Start Date: 2026-01-01
Estimated Completion Date: 2026-10
Participants
Target number of participants: 64
Treatments
Active_comparator: Metallic probe
Metallic UNC-15 periodontal probe (HuFriedy PCPUNC156)
Experimental: Plastic probe
Plastic UNC-15 periodontal probe (HuFriedy PCVO12PT)
Related Therapeutic Areas
Sponsors
Collaborators: Institut d'Investigació Biomèdica de Bellvitge
Leads: University of Barcelona

This content was sourced from clinicaltrials.gov