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Study on the application of vascularized fibula flap position frame in the repair of oral and maxillofacial bone defects

Study on the application of vascularized fibula flap position frame in the repair of oral and maxillofacial bone defects

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300079091
Enrollment
Unknown
Registered
2023-12-25
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Jaw defect caused by trauma or tumor

Interventions

Position frame group:A special position frame was used during the preparation of the vascularized fibula flap
No position frame group:No special position frame was used in the preparation of the vascularized fibula flap

Sponsors

West china hospital of stomatology, Sichuan university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age =18 years old and =75 years old, gender is not limited; (2) Jaw defects caused by various factors were confirmed by imaging and received surgical treatment with vascularized fibula flap transplantation; (3) Full organ and bone marrow function (4) The subjects voluntarily join the study, sign the informed consent, and comply with the visit and related procedures stipulated in the program.

Exclusion criteria

Exclusion criteria: (1) any active autoimmune disease or history of autoimmune disease, (2) Allergic disease, severe drug allergy, known to be allergic to macromolecular protein preparations; (3) Patients with serious medical diseases; (4) have an active infection, or an unexplained fever during screening, or use of systemic antibiotics within 1 week before signing informed consent; (5) The subject has active hepatitis B or C, or a known history of testing positive for human immunodeficiency virus (HIV) or a known history of acquired immunodeficiency syndrome (AIDS); (6) A prior history of a definite neurological or mental disorder, such as epilepsy or dementia; (7) have a clear history of drug abuse or a history of alcohol abuse within 3 months;

Design outcomes

Primary

MeasureTime frame
Ankle flexion;Knee flexion;Hip flexion;

Secondary

MeasureTime frame
patients' subjective experiences evaluation;

Countries

China

Contacts

Public ContactChen Jing

West china hospital of stomatology, Sichuan university

8048333@qq.com+86 189 8199 6484

Outcome results

None listed

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