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Clinical, microbiological and systemic anti-inflammation effects of antimicrobials combined with mechanical debridement on generalized aggressive periodontitis(GAgP):a randomised controlled trial

Impact of antimicrobials combined with mechanical debridement on generalized aggressive periodontitis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003925
Enrollment
Unknown
Registered
2013-08-06
Start date
2012-08-01
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

Generalized aggressive periodontitis

Interventions

Group 1:Local application of PERIOCLINE immediately after full-mouth mechanical treatment
Group 2:Local application of PERIOCLINE 3 months after full-mouth mechanical treatment
Group 3:Systemic antimicrobials combined with full-mouth mechanical treatment

Sponsors

Periodontic Dept., Peking University School of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 43 Years

Inclusion criteria

Inclusion criteria: 1. GAgP (according to the criteria of the 1999 international classification (Armitage 1999); 2. aged between 16 and 35 when first diagnosed with aggressive periodontal disease; 3. at least 20 teeth present; 4. good general health.

Exclusion criteria

Exclusion criteria: 1. suffered from any other systemic diseases (cardiovascular,pulmonary, liver, cerebral, diseases or diabetes); 2. pregnant or lactating females, or females of childbearing age not using a standard accepted method of birth control; 3. received antibiotic treatment in the previous 3 months; 4. received a course of periodontal treatment within the last 6 months; 5. required antibiotic pre-medication for the performance of periodontal examination and treatment; 6. allergic to minocycline, penicillin or metronidazole; 7. smoking; 8. not able to provide consent to participate in the study, or they do not accept the proposed treatment plan.

Design outcomes

Primary

MeasureTime frame
probing pocket depth (PPD);clinical attachment loss (CAL);Subgingival plaque microbiological outcome;

Secondary

MeasureTime frame
gingival recession;Full-mouth plaque score;Full-mouth bleeding score;blood routine test;blood glucose;blood lipid;IL-1beta;TNF-alpha;

Countries

China

Contacts

Public ContactXiangying Ouyang

Periodontic Dept., Peking University School of Stomatology

kqouyangxy@bjmu.edu.cn+86 13621050102

Outcome results

None listed

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