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Clinical Investigation of the Therapeutic Effect of Posterior Lumbar Interbody Fusion using Autologous Adipose tissue derived Stromal Vascular Fractio

Not Applicable
Conditions
Diseases of the musculoskeletal system and connective tissue
Registration Number
KCT0009328
Lead Sponsor
Bundang CHA General Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

patients requiring posterior lumbar interbody fusion surgery with 1 or 2 segments due to degenerative lumbar disease.

Exclusion Criteria

1) People suffering from acute infectious diseases
2) Those with bleeding diseases
3) Those who are pregnant, lactating, or of childbearing age and do not agree to maintain contraception during the clinical study period
4) Those diagnosed with malignant tumor
5) Those who have participated in other research within 4 weeks
6) Other persons judged by the PI to be unsuitable for participation in clinical research

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bone Fusion rate inside the cage evaluated by 3D-CT
Secondary Outcome Measures
NameTimeMethod
Bone Fusion rate, bone Fusion area ratio, and bone subsidence rate inside the cage evaluated by 3D-CT
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