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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032378
Enrollment
60
Registered
2018-04-25
Start date
2020-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar intervertebral disc degeneration associated with low back pain (containing lumbar disc herniation)

Interventions

Take NAC (300 mg / tablet) 2 tablets plus take 1 placebo tablet, total 3 tablets once 3 times a day for 24 weeks Take NAC (300 mg / tablet) 3 tablets once 3 times a day for 24 weeks Take 3 placebo tab

Sponsors

Keio University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All participants who agree with enrollment in this study and meet all the criteria as bellows; 1) Lumbar intervertebral disc degeneration (Phirrmann grade : 3, 4) or lumbar disc herniation in whom VAS score is over 5.0 point. 2) Regardless of patients with hospitalized or outpatinet. 3) Regardless of disease with primary or recurrence. 4) Agreement to stop anti-inflammatory analgesic except for an approved medicine.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Quantitative assessment of disc degeneration using Q-space imaging.

Countries

Japan

Contacts

Public ContactWatanabe Kota

Keio University School of Medicine Department of Orthopaedic Surgery

watakota@gmail.com03-3353-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026