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Special Drug Use Survey of HERNICORE 1.25 units for intradiscal injection in Patients with Lumbar Disc Herniatio

Not Applicable
Conditions
umbar Disc Herniation
Registration Number
JPRN-UMIN000034724
Lead Sponsor
SEIKAGAKU CORPORATIO
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
1862
Inclusion Criteria

Not provided

Exclusion Criteria

None

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Safety - Occurrence of adverse events and adverse reactions - Occurrence of post-treatment surgery for lumbar spinal instability at the same level of administration of HERNICORE Efficacy - Improvement of leg pain and low back pain - Occurrence of post-treatment surgery for lumbar disc herniation at the same level of administration of HERNICORE - Global assessment (physician) - Effects on long-term prognosis (e.g., recurrence of herniation, osteophyte formation, spinal canal stenosis)
Secondary Outcome Measures
NameTimeMethod
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