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Prospective cohort study of peri-implantitis treatment

Peri-implantitis patient cohort study: risk assessment and treatment strategy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066262
Enrollment
Unknown
Registered
2022-11-29
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

peri-implantitis

Interventions

Standardized systemic periodontal treatment:Not appropriate

Sponsors

Stomatological Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Adults aged 18-80 with autonomous ability; 2) At least one implant with probing depth >= 6mm together with the symptoms of peri-implantitis, including peri-implant bone loss (or peri-implant bone loss >= 2 mm compared to initial healing), bleeding on probing/ suppuration; 3)Be able to provide an informed consent form and completion of the questionnaires.

Exclusion criteria

Exclusion criteria: 1) Systemic disease that are known to affect soft tissue or bone; 2) History of radiotherapy for head and neck tumors; 3) Pregnancy; 4) Antibiotic use in the past 6 months; 5) Implants received treatment in the past 6 months; 6) Inability to be contacted over the phone during follow-up.

Design outcomes

Primary

MeasureTime frame
Peri-implant probing pocket depth;

Secondary

MeasureTime frame
Peri-implant alveolar bone resorption;

Countries

China

Contacts

Public ContactShulan Xu

Stomatological Hospital, Southern Medical University

xushulan_672588@smu.edu.cn+86 20 34304863

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026