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The influnce of different bone substitutes on the clinical effects of maxillary sinus floor elevation

The influnce of different bone substitutes on the clinical effects of maxillary sinus floor elevation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300072240
Enrollment
Unknown
Registered
2023-06-07
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

Dental defects with bone defect

Interventions

Bio-Oss ABBM:N/A
Bio-Oss collagen:N/A

Sponsors

Hospital of Stomatology, Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Patients needed to perform implantation, over 18 years old. 2.Patients underwent transalveolar maxillary sinus floor elevationand received simultaneous implant placement. 3.Patients were willing to supply the information.

Exclusion criteria

Exclusion criteria: 1.Patients with systemic disease unable to undergo the surgery. 2.Untreated periodontitis 3.With a history of receiving bisphosphonates 4.Smoke more than 10 per day 5.Patients lack of compliance or unwilling to participate in this study.

Design outcomes

Primary

MeasureTime frame
linear measurement;Success rate of implants;Volume of peri-implant bone remolding;—

Secondary

MeasureTime frame
Accuracy of implantation; Duration of surgery; OHIP-14;—

Countries

China

Contacts

Public ContactYe Ying

Hospital of Stomatology, Tongji University

onlinecrux@foxmail.com+86 21 6631 3725

Outcome results

None listed

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