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Clinical Outcomes of Absorbable Bone Repair Substitute Materials (Gufusheng®) in Real-World Applications

Clinical Outcomes of Absorbable Bone Repair Substitute Materials (Gufusheng®) in Real-World Applications

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103940
Enrollment
Unknown
Registered
2025-06-09
Start date
2025-06-16
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Bone fracture repair in various orthopedic surgeries

Interventions

Study Group:None

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients receiving Gufusheng® according to its indicated use cases, with an implantation duration of no less than 6 months.

Exclusion criteria

Exclusion criteria: 1.Cases with no postoperative follow-up data after receiving the product; 2.Cases where the product was not used for its intended bone-filling purpose.

Design outcomes

Primary

MeasureTime frame
Bone Fusion Rate at 6 Months Postoperatively;—

Secondary

MeasureTime frame
Skin wound healing;Vital Signs Monitoring;Localized tenderness at the fracture site;Spinal Percussion Tenderness;Safety Check;Incidence rate of complications;—

Countries

China

Contacts

Public ContactChao Chen

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

chenchao027@163.com+86 158 0275 8608

Outcome results

None listed

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