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Evaluation of the efficacy of the combination of medical care and patient 3A+2P in patients with periodontitis implantation

Evaluation of the efficacy of the combination of medical care and patient 3A+2P in patients with periodontitis implantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101354
Enrollment
Unknown
Registered
2025-04-23
Start date
2025-04-30
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

dental defect

Interventions

control group:For patients with periodontitis undergoing dental implants, routine nursing intervention is adopted: instruct the patients to pay attention to oral hygiene, inform them of the correct wa
test group:For patients with periodontitis undergoing implantation, a "3A + 2P" model combining medical staff, patients and doctors is adopted. (1) (Awareness) Enhance the oral care awareness of patie

Sponsors

Hospital of Stomatology, Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Indications: (1) Patients with periodontitis accompanied by missing teeth and undergoing implantable fixed denture restoration; (2) No acute inflammation in the oral cavity; (3) No smoking history or smoking less than 10 cigarettes per week; (4) Aged between 18 and 75 years old and without systemic diseases that affect the success rate of implantation; (5) After being fully informed of the treatment plan, the patient agreed to participate in this study, signed the informed consent form, and cooperated with regular follow-up visits and follow-ups.

Exclusion criteria

Exclusion criteria: (1) There is uncontrolled or poorly controlled periodontitis; (2) Suffering from serious cardiovascular, lung, liver, kidney and blood and endocrine system diseases; (3) Patients with bone tissue disorders, such as osteoporosis, osteomalacia, and osteosclerosis; (4) Mental abnormalities; (5) Severe infectious diseases; (6) Pregnant and lactating women; (7) Other circumstances that are not suitable for implant surgery.

Design outcomes

Primary

MeasureTime frame
Probing depth;Implant survival rate;Peri-implant bone loss;Per-implant soft tissue status: GI, PI, PD, modified bleeding index on probing;

Secondary

MeasureTime frame
The satisfaction of patients;

Countries

China

Contacts

Public ContactHuang Jianfang

Hospital of Stomatology, Wuhan University

12213694@qq.com+86 135 0714 2839

Outcome results

None listed

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