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A prospective randomized controlled study on microsurgery for peri-implantitis

A prospective randomized controlled study on microsurgery for peri-implantitis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081133
Enrollment
Unknown
Registered
2024-02-23
Start date
2023-07-15
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

peri-implantitis

Interventions

experimental group:Microsurgical therapy + GBR
control group:periodontal flap surgery + GBR

Sponsors

Stomatological Hospital Affiliated to Nanjing University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age range from 18 to 65 years old, regardless of gender; 2.The diagnosis of peri-implant inflammation meets the general diagnostic criteria; 3.a probing pocket depth (PPD) =5 mm with bleeding on probing (BOP)/suppuration (SUP), a radiographic intra-osseous defect =3 mm;

Exclusion criteria

Exclusion criteria: 1. a history of peri-implantitis surgery on the test tooth; 2. Peri-implantitis and severe bone destruction due to poor implant placement or other reasons for implant retention; 3. Patients with systemic diseases that affect periodontal healing; 4. During pregnancy or breastfeeding; 5. Patients with poor compliance; 6. Patients who have used medications affecting periodontal conditions within the past 6 months; 7. Patients with smoking habits of = 10 cigarettes per day; 8. patients with medicated osteomyelitis; 9. various subjects capable of causing artifacts on oral imaging;

Design outcomes

Primary

MeasureTime frame
probing depth;

Secondary

MeasureTime frame
gingival recession;bleeding on probing;

Countries

China

Contacts

Public ContactHouxuan Li

Nanjing Stomatological Hospital,Affiliated Hospital of Medical School,Nanjing University,Nanjing,China

lihouxuan3435_0@163.com+86 187 9586 3036

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026