The Selective Intraperineural Nerve Root Block Study
Starting soon · Not applicable · Has a placebo group
Conditions studied: Radiculopathy Lumbar, Radiculopathy Sacral, Radiculopathy Multiple Sites, Herniated Disc, Foraminal Stenosis
In brief
Before lumbosacral decompression surgery for radicular pain, selective nerve root block(SNRB) is a common procedure to identify the responsible compressed nerve root(RCNR) and predict surgical outcomes. However, the diagnostic accuracy of conventional SNRB is unsatisfactory, especially in terms of specificity. The main limitation is the uncontrolled distribution of anesthetics during injection: when anesthetics spread to surrounding soft tissues instead of acting directly on the RCNR, false-negative results may occur with persistent radicular pain; when anesthetics diffuse to two or more nerve roots including the RCNR, false-positive results may occur even if a normal nerve root is punctured, leading to misdiagnosis. This study aims to evaluate the diagnostic accuracy of a novel three-dimensional computed tomography multiplanar volume reconstruction (3D-CT MPVR) guided selective intraperineural nerve root block(SINRB) for identifying the RCNR in patients with lumbosacral radicular pain. The investigators hypothesize that this technique will achieve higher diagnostic specificity and overall accuracy than conventional SNRB, by ensuring anesthetics are delivered directly to the target nerve root. This improvement will help clinicians make more accurate surgical plans, achieve better targeted decompression, and ultimately improve postoperative pain relief and functional recovery for patients. The main research questions to be addressed in this study are: * What is the procedural success rate of SINRB? * Whether SINRB may cause clinically detectable nerve injury? * Whether sciatica is relieved after SINRB when only the responsible compressed nerve root is blocked? * Whether sciatica is relieved after SINRB when only a normal unaffected nerve root is blocked? Participants will: * Undergo one or two SINRB procedures and a single-level lumbar decompression surgery * Get assessment of pain, mobility disorder and neurological function
Key facts
- Study ID
- NCT07531485
- Run by
- Xi'an Honghui Hospital
- People needed
- 80
- Starts
- 2026-04-13
- Expected to finish
- 2027-01-01
- Last updated by the study team
- 2026-04-15
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Unilateral sciatica >1 month with activity/daily life impairment.
- Suspected L5/S1 root compression at L4-5/L5-S1 with unconfirmed pain correlation, including disc herniation (MSU 1-B/1-A/2-A), lateral recess/foraminal stenosis (Lee grade 2/3), atypical sciatica, or imaging-exam inconsistency.
- Candidates for single-segment, single-root lumbar decompression, electing surgery after informed consent.
You may not qualify if…
- No significant pre-SINRB/surgery pain, or weakness/numbness as primary symptom.
- Unidentifiable responsible compressed nerve root (RCNR) per surgery.
- Suspected compression of the same nerve root at more than one segment.
- Pregnancy, active malignancy, or surgical contraindications.
- Inability to cooperate with assessment due to comorbidities or dysfunction.
Where it is running
- Xi'an Honghui Hospital (North Campus) — Xi'an, Shaanxi, China
Full record on ClinicalTrials.gov
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