跳至主要内容
临床试验/CTRI/2023/10/058286
CTRI/2023/10/058286招募中2 期

A Multi-Center, Prospective, Open-Label, Assessor-Blinded, Randomised, Controlled, Non-Inferiority, Pivotal Clinical Investigation to evaluate the Performance and Safety of 3-D Scaffold Matrix – a Class C Medical Device Bone Void Filler as a Bone Graft Substitute in Orthopaedic Surgery - NI

EffecMed Pvt. Ltd.0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1 Patients between the age of 18 and 65 years both inclusive with any of the following
  • a. Requiring bone grafting after post-traumatic or surgically created bone defects afflicting the long bones and extremities.
  • b. Gap defects 6mm and 25 mm
  • c. Traumatic, open and closed fracture
  • d. Open and closed fractures - traumatic, closed, depression fracture of the proximal tibia (limited to AO type B2 and B3)
  • e. Cavitary defects in benign and low-grade malignant bone tumours.
  • f. Bone void created during surgery.
  • g. Bone disease i.e. osteogenesis imperfecta, cancer, osteoporosis, Paget disease
  • 2. Negative for HIV and HBsAg.
  • 3. Written informed consent obtained before any study-related activities.
  • 4. Communicative ability to understand the procedure and participate in the study and comply with the follow up.

排除标准

  • Patient will be excluded from the study, if they have any of the following
  • 1. Critical size defect below 5 mm
  • 2. Critical size defect more than 26 mm
  • 3. Polytrauma bone injuries
  • 4. Excessive destruction of bone through and through defects, excessive thinning of lower border
  • 5. Injury leading to debridement interval more than 12 h
  • 6. Compartment syndrome
  • 7. Pathologic fracture
  • 8. Chronic pain disease
  • 9. Malignancy
  • 10. Chronic cortisone intake
  • 11. Clinically significant or unstable medical or surgical condition that may preclude safe and complete study participation
  • 12. Pre-existing calcium metabolism disorder Hypercalcemia
  • 13. Known hyperthyroidism or autonomous thyroid adenoma
  • 14. Irreversible coagulopathy or bleeding disorder
  • 15. Metastatic cancer
  • 16. Active infection at the site of implantation
  • 17. History of bone marrow disorders
  • 18. Active malignancy, cellulitis, osteomyelitis, bone metastasis, and other bone metabolic diseases.
  • 19.Primary bone tumour and contraindications in performing an Xray or CT scan
  • 20. Women of childbearing potential who are, or plan to become, pregnant during the time of the study.
  • 21.With known autoimmune disease, such as Addison disease, Myasthenia gravis, Pernicious anaemia, Reactive arthritis, Rheumatoid arthritis, Sjogren syndrome, Systemic lupus erythematosus, Dermatomyositis, Grave disease, Hashimotos thyroiditis, and Type 1 diabetes mellitus.
  • 22. Physical or psychological condition that contraindicates the use of an investigational device or render the patient at high risk from treatment complications.
  • 23. Concurrently participating in other clinical trials or within last 1 month.

研究者

发起方
EffecMed Pvt. Ltd.

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