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Repair of Bone Defect by Auto Bone Marrow Concentrates Combined with beta-TCP

Repair of Bone Defect by Auto Bone Marrow Concentrates Combined with beta-TCP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15006799
Enrollment
Unknown
Registered
2015-07-21
Start date
2013-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Alveolar Cleft

Interventions

experiment group:uto bone marrow concentrates combined with beta-TCP graft

Sponsors

Plastic Surgery Hospital, Chinsese Academy of Medical Sciences & Peking Union Medical
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 27 Years

Inclusion criteria

Inclusion criteria: 1) 10-40 year old male or female patients with bone defect in non-load-bearing area; 2) The defects were in the range of 1-3cm. (Craniofacial bone, jaw bone defects and deformities); 3) Patients and their families voluntarily underwent surgery, postoperative radiological examinations, follow-up and postoperative rehabilitation; 4) Patients and their families need to personally read, understand and sign the relevant voluntary informed consent.

Exclusion criteria

Exclusion criteria: 1) Bone defects larger than 3cm or bone defects in weight-bearing site; 2) Patients with obvious abnormality in routine examination; 3) The heart, lungs, brain, kidneys and other vital organ function or hematopoietic function is severely impaired; 4) Patients with obvious malnutrition; 5) Patients with mental and neurological disorders that can not follow instructions of doctors; 6) Recipient site have extensive scarring or poor blood supply caused by extensive radiotherapy or surgery or multiple trauma; 7) Patients received BMP growth factors or other bone growth promoting factor therapy; 8) Patients with a history of metabolic disease that may affect bone regeneration (such as osteoporosis, osteomalacia); 9) Patients received radiotherapy, chemotherapy, immunosuppressive or anticoagulant therapy recently; 10) Patients with systemic or local infection; 11) Patients with allergic constitution or allergic to drugs, regents or materials (TCP) used in the trial; 12) Patients with alcohol or addictive drugs dependence; 13) Patients participating in other clinical study currently.

Design outcomes

Primary

MeasureTime frame
bone formation;continuity of alveolar bone;

Secondary

MeasureTime frame
bone density;donor site damage;

Countries

China

Contacts

Public ContactYilin Cao
yilincao@163.com+86 13701802351

Outcome results

None listed

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