Long-term safety follow-up study of evaluating active biological bone for bone defect repair

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400091974

Enrollment

Unknown

Registered

2024-11-06

Start date

2024-11-06

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Bone defect

Interventions

experimental group:Active biological bone

control group:Traditional artificial bone

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Patients aged 18 to 75, one year years old (including 18 and 75 years old), gender is not limited; 2) Patients with bone defects caused by trauma or surgery that do not affect the stability of bone structure and need repair by bone transplantation; 3) Patients who voluntarily participate in the informed consent form and sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1) Patients with a history of severe allergic reaction; 2) Patients with abnormal immune function; 3) critically ill patients such as advanced tumors; 4) Patients judged by other investigators as unable to complete or unsuitable to participate in the study.

Design outcomes

Primary

Measure	Time frame
Healing;	—

Countries

China

Contacts

Public ContactLi Zhong

Xi’an Honghui Hospital

lizhong0607@126.com+86 139 9288 8878

Outcome results

None listed

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