Saftey and effectiveness evaluation of a multi-functional modularized prosthesis in sternal resection and reconstruction

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037203

Enrollment

Unknown

Registered

2020-08-27

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-10-13

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

Conditions

undergoing sternal resection and reconstruction for sternal malignancy or infection

Interventions

experimental group:multi-functional modularized prosthesis

control group:platinum plate

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18-70 years; 2) Undego sternal resection and reconstruction surgery; 3) Signed written informed consent.

Exclusion criteria

Exclusion criteria: 1) Presence of severe osteoporosis and other bone diseases; 2) Malnutrition; 3) Previous history of chemotherapy or radiotherapy; 4) Presence ofother surgical contraindications.

Design outcomes

Primary

Measure	Time frame
survival of prosthesis;	—

Countries

China

Contacts

Public ContactHaifeng Wang

Shanghai Pulmonary Hospital

Nautilus2316@163.com+86 13651987198

Outcome results

None listed

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