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Randomized, placebo-controlled, double-blind comparative study of N-Acetylcysteine for the treatment with intervertebral disc degeneration.

Not Applicable
Completed
Conditions
umbar intervertebral disc degeneration associated with low back pain (containing lumbar disc herniation)
Registration Number
JPRN-UMIN000032378
Lead Sponsor
Keio University School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

1) Severe combined complications of heart, liver and blood diseases. 2) Patients with surgical treatment that attending physician consider having impact on the results. 3) Three times higher of AST/ALT before administration of NAC 4) Currently taking NAC or supplement containing NAC. 5) Allergy for NAC 6) Women who are during pregnancy, under lactation, have a possibility to pregnancy, and who hope pregnancy. 7) Previous spine surgery 8) Incompetent patients judged by attending doctor

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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