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Platelet activation and platelet-leukocyte aggregate in patients with generalized aggressive periodontitis

Platelet activation and platelet-leukocyte aggregate in patients with generalized aggressive periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-IOC-15007663
Enrollment
Unknown
Registered
2015-12-27
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Aggressive periodontitis

Interventions

Generalized aggressive periodontitis group vs Healthy population :Active periodontal treatment (APT) includes oral hygiene instruction, supragingival scaling, and quardrant-based subgingival scaling a

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: The diagnostic criteria forgeneralized aggressive periodontitis is according to the classification proposed at the International Workshop for the Classification of Periodontal Diseases and Conditions in 1999. The inclusion criteria of the generalized aggressive periodontitisgroup are: 1. The onset of the periodontal disease occurred under 35 years old; 2. At least 8 teeth with probingdepth (PD)over 5 mm and attachment loss (AL) over 3 mm, three or more of which are not first molars or incisors; 3. Radiographs showed alveolar bone loss; 4. At lease 20 functional teeth remained, at least 1 molar remained in every quadrant. In addition, periodontal healthy subjects are selected from the staffs and students at Peking University School and Hospital of Stomatology; the inclusion criteria are: 1. PD <=3 mm; 2. The percentage of sites with bleeding on probing (BOP) is<10%; 3. No attachment loss (AL); 4. No bone loss visible on radiographs.

Exclusion criteria

Exclusion criteria: 1. Less than 18 years old; 2. Current or previous smoker; 3. The presence of systemic disease or pregnant; 4. History of periodontal therapy or antimicrobial therapy within 6 months, or usage of any medication (including oral contraceptive drugs) within 3 months.

Design outcomes

Primary

MeasureTime frame
Probing depth;Attachment loss;Bleeding index;White blood cell count;Neutrophile granulocyte percent;Neutrophile granulocyte count;Platelet count;Platelet distribution width;Platelet large cell ratio;Mean platelet volume;CD62P;PAC-1;S100A9;Platelet-leukocyte aggregate;IL-1 beta;IL-6;CRP;TNF-alpha;sCD62P;sCD40L;beta-TG;PF-4;Vov willebrand factor;CD40L;Platelet-neutrophil aggregate;Platelet-monocyte aggregate;Platelet-lymphocyte aggregate;

Secondary

MeasureTime frame
Triglyceride;Total cholesterol;High density lipoprotein;Low density lipoprotein;Fasting glucose;

Countries

China

Contacts

Public ContactMeng Huanxin
kqhxmeng@bjmu.edu.cn0086-10-82195368

Outcome results

None listed

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