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clinical efficacy of immediate implantation after extensive buccal bone defect in maxillary molar extraction socket: a prospective cohort study

clinical efficacy of immediate implantation after extensive buccal bone defect in maxillary molar extraction socket: a prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106314
Enrollment
Unknown
Registered
2025-07-22
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Implantology

Interventions

Case series:NA

Sponsors

Shanghai Ninth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18–70 years (inclusive), any sex. 2. Periodontally healthy, with at least one adjacent tooth that is healthy and unrestored. 3. Tooth scheduled for extraction with 50 % of the root length. 5. Horizontal gap between the socket wall and the implant > 2 mm, and at least 4 mm of residual bone height apical to the socket. 6. Willing to participate and has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with bone-metabolic disorders (e.g., osteoporosis, Paget’s disease) or who have taken medications/substances that markedly affect bone metabolism (e.g., corticosteroids, bisphosphonates) within the 3 months prior to enrollment. 2. Patients with severe cardiac disease, coagulopathy, or any other condition deemed unsuitable for surgery by the investigators. 3. Patients with abnormal hepatic or renal function (ALT or AST > 1.5 × upper limit of normal, or serum creatinine above normal). 4. Patients with poorly controlled diabetes (fasting glucose >= 8 mmol/L) or poorly controlled hypertension (systolic >= 160 mmHg and/or diastolic >= 100 mmHg). 5. Patients with prior radiotherapy to the head and neck region. 6. Heavy smokers (>= 10 cigarettes per day). 7. Patients with acute apical periodontitis, active periodontal disease, a history of refractory periodontitis, or active infection. 8. Patients with poor oral hygiene who are unable to maintain adequate oral care. 9. Patients unable to undergo oral imaging required for outcome assessment. 10. Women of child-bearing potential who are pregnant, planning pregnancy, or lactating; men whose partners are planning pregnancy. 11. Patients with severe psychiatric disorders. 12. Patients who have participated or are participating in another drug or device clinical trial within the past 3 months. 13. Patients with poor compliance or otherwise deemed unsuitable for inclusion by the investigators.

Design outcomes

Primary

MeasureTime frame
bone height;

Secondary

MeasureTime frame
Bone Width;Soft tissue increment;

Countries

China

Contacts

Public ContactYingxin Gu

Shanghai Ninth People's Hospital

zcn1114@163.com+86 21 5331 5299

Outcome results

None listed

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