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The evaluation of leadoss bone level dental implants with simultaneous maxillary sinus floor elevation: A prospective, single-group clinical trial

The evaluation of leadoss bone level dental implants with simultaneous maxillary sinus floor elevation: A prospective, single-group clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068034
Enrollment
Unknown
Registered
2023-02-03
Start date
2023-02-02
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

dentition defect

Interventions

Sponsors

Wuhan University Stomatological Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Understand the process of implant repair and sign the preoperative informed consent, and be able to review as required; 2. Aged 18-75 years, both sexes; 3. Maxillary molars with missing teeth, residual bone height of 5mm-8mm, bone width of at least 7.2mm, and maxillary sinus floor elevation (elevation of 2mm-4mm); 4. There was no obvious inflammation, cyst or septum in the maxillary sinus; 5. The bone and bone mass of the missing tooth area meet the requirements of simultaneous implant implantation; 6. There was no obvious inflammation or disease in the oral mucosa and soft tissue of the implant area, and no periodontal or apical inflammation in the adjacent teeth.

Exclusion criteria

Exclusion criteria: 1. Patients with systemic diseases that may affect postoperative healing and/or osseointegration, such as uncontrolled diabetes, hypertension, etc.; 2. Systemic or local bone diseases, such as bone tuberculosis, osteitis, bone tumors, etc.; 3. Long-term use of special drugs that may affect postoperative healing or bone union; 4. Patients with contraindications of oral surgery; 5. Acute and chronic inflammation, cyst, and septum in the maxillary sinus; 6. Patients who received radiotherapy or chemotherapy in the past 3 years; 7. Uncontrolled periodontitis; 8. People who are dependent on alcohol, drugs, tobacco, or other drugs; 9. Participated in other clinical studies at the same time or participated in other clinical studies within the last 3 months; 10. Other conditions that the investigator considers inappropriate for the trial.

Design outcomes

Primary

MeasureTime frame
Implant success at 1 year after implant repair;

Secondary

MeasureTime frame
Implant stability;Evaluation of peri-implant soft tissue health;Vertical bone resorption;

Countries

China

Contacts

Public ContactShi Bin

Wuhan University Stomatological Hospital

shibin_dentist@whu.edu.cn+86 138 0864 3395

Outcome results

None listed

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