Last updated: February 24, 2024
Sponsor: Istanbul University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Mucositis
Periodontitis
Treatment
Labrida BioClean
EMS Handy 3.0 Perio Premium
Clinical Study ID
NCT06287957
IU-DHF-AG-01
All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Presence of peri-implant mucositis around at least one implant,
- Being over 18 years old,
- Being psychologically suitable,
- The teeth adjacent to the relevant implant are natural teeth,
- Having at least 1 implant in the maxillary or mandibular posterior region (teeth 4, 5, 6 and 7) and a cemented prosthesis that is not connected to other implants or teeth asits superstructure,
- Probing depth longer than 3 mm and shorter than 5 mm,
- Evidence of bleeding is required on probing.
Exclusion
Exclusion Criteria:
- Pregnancy
- History of chemotherapy and/or radiotherapy received in the past or currently beingreceived,
- Bone loss around the implant,
- Presence of an implant in the area adjacent to the relevant implant,
- Dentures combined with other implants or teeth,
- Screw-retained prostheses
- Uncontrolled diabetes
Study Design
Total Participants: 54
Treatment Group(s): 2
Primary Treatment: Labrida BioClean
Phase:
Study Start date:
March 01, 2024
Estimated Completion Date:
February 15, 2025
Study Description
Connect with a study center
Istanbul University
Istanbul, Fatih 34080
TurkeyActive - Recruiting
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