Radicular Low Back Pain

2

Review clinical trials related to Radicular Low Back Pain. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

R³ Rehab Pathway Versus Usual Care After Lumbar Radicular Surgery

The R³ trial is a multicentre cluster randomized controlled trial evaluating an evidence-based, person-centred rehabilitation pathway for patients undergoing lumbar surgery for radicular pain. The pathway includes structured pre-, peri-, and postoperative rehabilitation, early postoperative mobilization, case management, early return-to-work (RTW) guidance, and patient empowerment. Clusters (hospitals) are randomized to implement the R³ pathway (intervention) or continue usual care (control). The primary aim is to determine whether the R³ pathway reduces time to return to work compared with usual care.

Participants needed: 480
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Universitaire Ziekenhuizen KU LeuvenUpdated: May 5, 2026Locations: 16
Eligibility criteria

Radicular pain (for ≥ 6 weeks prior to screening), with a clear indication for l... [+5]

Lumbar surgery performed for malignant disease, spinal fracture, infectious spin... [+4]

Status: Not yet recruiting

The Role of Temporal Changes in Pain Response After Transforaminal Epidural Steroid Injection on Treatment Success

Transforaminal epidural steroid injection (TFESI) is a commonly used minimally invasive procedure for the treatment of lumbar radicular pain secondary to disc herniation. Although TFESI has been shown to provide significant pain relief in a substantial proportion of patients, the onset, duration, and temporal pattern of pain relief after the procedure vary considerably among individuals. The relationship between early pain response patterns and long-term treatment success remains poorly understood. This prospective observational study aims to evaluate whether temporal changes in pain intensity following TFESI, particularly during the early post-procedural period, are associated with clinical treatment success at mid- and long-term follow-up. Pain intensity will be assessed using the Numeric Rating Scale (NRS) at predefined time points following the procedure, and treatment success will be defined as a ≥50% reduction in NRS score compared with baseline.

Participants needed: 120
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Marmara UniversityUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Age between 18 and 65 years [+3]

Presence of spondylolisthesis, scoliosis, or lumbar spinal stenosis accompanying... [+5]