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An exploratory study on the clinical efficacy of air-powder abrasion combined with ultrasonic therapy in treating peri-implant diseases.

An exploratory study on the clinical efficacy of air-powder abrasion combined with ultrasonic therapy in treating peri-implant diseases.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123855
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

peri-implant mucositis or peri-implantitis

Interventions

control group:Subgingival ultrasound
experimental group:subgingival sandblasting combined with ultrasound

Sponsors

Beijing Stomatological Hospital , Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70, of either gender, with at least one implant in the mouth, who has completed the restoration of the superstructure and is now bearing load; 2. The probing depth around the implant (PPD) is <=5 mm, and X-ray shows that the absorption of the alveolar crest bone is ?4mm. 3. There are no sinus or occlusal trauma around the implant; 4. The patient is in good overall health with no evident systemic diseases; 5. No smoking or smoking less than 10 cigarettes per day;

Exclusion criteria

Exclusion criteria: 1. Individuals with mental disorders or intellectual disabilities; 2. Pregnant and lactating women; 3. Implant loosening.

Design outcomes

Primary

MeasureTime frame
probing depth;

Secondary

MeasureTime frame
Crestal Bone Level;Bleeding on probing;Clinical attachment loss;Plaque Index;

Countries

China

Contacts

Public ContactXu Xiaoxi

Beijing Stomatological Hospital, Capital Medical University

xuxiaoxi_930@163.com+86 10 5709 9671

Outcome results

None listed

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