Follow-up study of LDH patients participated in the Phase II/III study (6603/1021) and Phase III study (6603/1031) of condoliase (SI-6603)
Not Applicable
- Conditions
- umbar Disc Herniation
- Registration Number
- JPRN-UMIN000015221
- Lead Sponsor
- SEIKAGAKU CORPORATIO
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 356
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who have not given their written informed consent to participate in the follow-up study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method