Skip to content

Study of PLGA-Mg Material in Clinical Orthopedics

Randomized, Double Blind Trial of Study of PLGA-Mg Material in Clinical Orthopedics

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03060655
Enrollment
40
Registered
2017-02-23
Start date
2016-08-31
Completion date
2018-03-31
Last updated
2017-02-23

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

Conditions

Fracture Dislocation

Keywords

PLGA-Mg, fracture, fixation, union

Brief summary

The different proportion samples of PLGA-Mg were made in this study. Then, they would be placed in the femoral condyle of the New Zealand rabbits. The appropriate proportion of PLGA-Mg is obtained after the experiment, which will be used to make the plate or screw to fix the fragments. Then, the clinical role for bone will be assessed.

Detailed description

The deposition of calcium could be facilitated by the increase of magnesium, which played an important role in fracture union. However, its degradation may be completed before the fracture line was disappeared. In addition, the hydrogen may be released during degradation. Thus, its clinical popularization was limited. As a new polymer material, poly lactic-co-glycolic acid (PLGA) has been widely used clinically. The hydrolytic production of PLGA was acidic, which could neutralize the alkalinity of production degraded from magnesium. In addition, it was a long time before the total accomplishment of degradation of PLGA, which may postpone the degradation of magnesium. The different proportion samples of PLGA-Mg were made in this study. Their physical and chemical properties were analyzed to estimate its safety of implantation. Then, they would be placed in the femoral condyle of the New Zealand rabbits. The osteogenesis and complication of samples are examined to select an appropriate proportion of PLGA-Mg is obtained. Then, the PLGA-Mg material will be used to fix the fracture of human as a fixation. The review of the patients will be conducted to assess its clinical role.

Interventions

BIOLOGICALPLGA-Mg material

The PLGA-Mg material was used to accomplish the fixation of fragments. Then, the clinical outcome was assessed.

BIOLOGICALtitanium alloy

Traditional fixation was titanium alloy. the clinical outcome was assessed.

Sponsors

Hebei Medical University Third Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-65 years old * Closed fracture * Sign the agreement of the experiment

Exclusion criteria

* Pathologic fracture * Open fracture * Refused to participate * Follow-up insufficient 12 months

Design outcomes

Primary

MeasureTime frame
fracture union time4 months

Secondary

MeasureTime frameDescription
complication1 monthsnonunion, toxicity

Countries

China

Contacts

Primary ContactYingze Zhang, M.D
yzzhangdr@126.com+8613313012888

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026