A Phase III Study of SI-6603 in Patients with Lumbar Disc Herniatio
Not Applicable
- Conditions
- umbar Disc Herniation
- Registration Number
- JPRN-UMIN000007239
- Lead Sponsor
- SEIKAGAKU CORPORATIO
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients who have undergone lumbar operation in the past 2.Patients with diseases that can affect the results of this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change from baseline of pain due to lumbar disc herniation
- Secondary Outcome Measures
Name Time Method