A Study of SI-6603 in Patients With Lumbar Disc Herniation

See also
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Enrolling by invitation	`NCT05444751` - GA + ESP vs. SA + ESP in Lumbar Decompression Surgeries	Phase 3
Completed	`NCT02700451` - Post-op Acetaminophen vs NSAID Use on Lumbar Spinal Fusion Outcomes	N/A
Active, not recruiting	`NCT03733626` - Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease	N/A
Recruiting	`NCT04042844` - A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD)	Phase 2
Completed	`NCT05345249` - Erector Spinae Plane Block as Pain Management After Lumbar Fusion Surgery	Phase 4
Active, not recruiting	`NCT03060434` - Pentoxifylline and Lumbar Radiculopathy	Phase 4
Withdrawn	`NCT02852187` - Single Center Study Comparing MOBIS II ST vs MOBIS PEEK	N/A
Completed	`NCT04062942` - The Six-Minute Walking Test (6WT) and Timed-Up-and-Go (TUG) Test as Measures of Objective Functional Impairment in Patients Undergoing Interlaminar or Transforaminal Epidural Steroid Injection for Lumbar Degenerative Disc Disease (DDD)
Recruiting	`NCT03745040` - Liposomal Bupivacaine in One-level Instrumented Posterior Spinal Fusion	Phase 4

NCT number	NCT02421601
Study type	Interventional
Source	Seikagaku Corporation
Contact
Status	Completed
Phase	Phase 3
Start date	March 2015
Completion date	February 2018

A Study of SI-6603 in Patients With Lumbar Disc Herniation

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms