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Microbial Investigation of Soft Tissues in Oral Inflammation

Microbial Investigation of Soft Tissues in Oral Inflammation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107795
Enrollment
Unknown
Registered
2025-08-19
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

periapical periodontitis

Interventions

periapical periodontitis:None
Control:None
Chronic periodontitis:None

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Age 18–70 years and indicated for tooth extraction on the basis of clinical examination; 2.Provision of written informed consent and a complete medical history; 3.Commitment to full trial participation, including attendance at all scheduled visits and completion of all study procedures; 4.Absence of systemic or topical antiviral therapy within the preceding 3 months; 5.Presence of >= 20 functional natural teeth; absence of rampant caries, active mucosal disease, acute oral inflammation, removable prostheses, or fixed/removable orthodontic appliances.

Exclusion criteria

Exclusion criteria: 1.Presence of severe systemic disease (as judged by the clinical investigator), including but not limited to cardiac arrhythmia, uncontrolled hypertension, diabetes mellitus, hepatitis of any etiology, or renal failure; 2.Pregnant or lactating women, or those planning pregnancy during the study period (self-reported); 3.History of head-and-neck radiotherapy or use of bisphosphonates, denosumab, or similar agents; 4.Current smoker (any form of tobacco use); 5.Periodontal therapy or antiviral medication within the preceding 3 months; 6.Any psychiatric disorder or other condition resulting in legally recognized diminished capacity to provide consent; 7.Lack of legal capacity to consent or refusal to participate; 8.Any additional condition that, in the opinion of the investigator, would preclude safe or compliant study participation.

Design outcomes

Primary

MeasureTime frame
Probing Depth;Maximum diameter of apical lesion on X-ray;

Countries

China

Contacts

Public ContactShen Yuqing

Zhongshan Hospital, Fudan University

shen.yuqing@zs-hospital.sh.cn+86 21 64041990

Outcome results

None listed

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