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Clinical application of additive manufacturing of customized porous tantalum implants

Clinical application of additive manufacturing of customized porous tantalum implants

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022731
Enrollment
Unknown
Registered
2019-04-23
Start date
2018-12-01
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

Bone diseases

Interventions

Case series:tantalum implants surgery

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged = 15 years old male and female; 2. Metal prosthesis/pad should be used for patients with dysplasia/bone disease/trauma/artificial joint failure/internal fixation failure, etc.; 3. Sign the informed consent form and agree to be enrolled in the study and ensure to complete follow-ups.

Exclusion criteria

Exclusion criteria: 1. Patients with active infection, severe coagulopathy, etc. that are not suitable for surgery; 2. Patients with severe cardiopulmonary disease that can not tolerate the operator; 3. Patients who can not cooperate with the treatment due to mental disorders or mental retardation; 4. Patients who can not complete postoperative follow-ups on time; 5. Patients who has history of metal allergy.

Design outcomes

Primary

MeasureTime frame
incidence of adverse reactions: postoperative incision infection, periprosthetic infection, deep vein thrombosis, postoperative hyperthermia, vascular nerve injury, etc.;Surgical site joint function score and SF36 quality of life score;tantalum implant position measured by radiographs: whether the implant is loose or sinking;

Secondary

MeasureTime frame
changes in blood test indicators;

Countries

China

Contacts

Public ContactYang Liu

The First Affiliated Hospital of Army Medical University

arthro@126.com+86 23 68765280

Outcome results

None listed

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