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Study on the Repair Effect of Calcium Silicon Bioceramic Bone Repair Material for Filling Bone Defects in Jaw Cystectomy

Study on the Repair Effect of Calcium Silicon Bioceramic Bone Repair Material for Filling Bone Defects in Jaw Cystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103463
Enrollment
Unknown
Registered
2025-05-29
Start date
2025-06-03
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Bone defect filling during mandibular cyst removal surgery

Interventions

Test group:Calcium-silicon bioceramic bone repair material filling repair

Sponsors

Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Age range of 18-70 years old (including upper and lower limits), gender is not limited; 2.The maximum diameter of the jawbone cyst is between 2cm-4cm, and the lingual bone wall is intact; 3.The number of affected teeth is 2-3; 4.Removal of jaw cyst combined with guided bone regeneration technology is required for bone defect repair; 5.Participants voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with cyst infection; 2.Patients with polycystic, multiple or recurrent jaw cysts; 3.Patients with maxillofacial space occupying lesions or malignant tumors in other parts of the body; 4.Patients with a history of acute periapical periodontitis, progressive periodontal disease, and refractory periodontitis; 5.Patients with bone metabolism disorders (such as osteoporosis, abnormal osteoarthritis, etc.), or those who have taken drugs or products that can significantly affect bone metabolism (such as steroids, bisphosphonates, etc).within the past 3 months before enrollment; 6.Patients with a history of head and neck radiotherapy; 7.Patients who are unable to undergo oral imaging examinations and those who may experience dental imaging artifacts that affect outcome evaluation; 8.Patients who have taken anticoagulant drugs or have abnormal coagulation function in the past 3 months and are deemed unsuitable for surgery by researchers; 9.Patients with abnormal liver and kidney function (ALT and AST values exceeding 1.5 times the upper limit of normal, or creatinine exceeding normal); 10.Poorly controlled diabetes (fasting blood glucose >= 8 mmol/L), poorly controlled hypertension (systolic blood pressure >= 160 mmHg and/or diastolic blood pressure >= 100 mmHg); 11.Pregnant and intending pregnant women of childbearing age and lactating women; 12.Patients who smoke heavily (>= 10 cigarettes/day); 13.Patients with severe mental illness, alcohol or drug abuse; 14.The patient has participated in or is currently participating in clinical trials of other drugs or devices within the past 3 months; 15.Other patients deemed unsuitable for inclusion by researchers.

Design outcomes

Primary

MeasureTime frame
Evaluate the changes in bone mass in the bone defect filling area after mandibular cyst removal at 3 and 6 months post surgery compared to 1 day post surgery using CBCT imaging;

Secondary

MeasureTime frame
Wound healing status;

Countries

China

Contacts

Public ContactGuo Jun

Sichuan Provincial People's Hospital

guojun-001@qq.com+86 28 8739 3825

Outcome results

None listed

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