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临床试验/NCT07531485
NCT07531485尚未招募不适用

Feasibility, Safety and Diagnostic Accuracy of Selective Intraperineural Nerve Root Block for Identifying Compressed Nerve Root in Lumbosacral Radicular Pain. A Prospective Cohort Study

Xi'an Honghui Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年4月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
80
试验地点
1
主要终点
The change from baseline in standing impairment

研究概览

简要总结

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

详细描述

[Background] It has been reported that approximately 85% of sciatica cases result from nerve root compression secondary to lumbar disc herniation or lumbar spinal stenosis, a clinical entity defined as radicular pain that manifests as radiating pain involving the buttocks and lower extremities. For patients with an inadequate response to conservative management, surgical decompression of the compressed nerve root serves as a conventional and highly effective therapeutic option. Furthermore, if the pain generator can be confirmed to arise from a single nerve root, targeted single-level decompression of that individual nerve root is generally sufficient for pain relief. However, limitations of conventional imaging examinations coupled with overlapping innervation territories of multiple lumbosacral nerve roots often make accurate identification of the symptomatic compressed nerve root challenging in certain patient populations. Misidentification of the pathological nerve root may consequently lead to surgical failure. To address this clinical dilemma, diagnostic selective nerve root block (SNRB) is regarded as the most valuable adjunct modality. In routine clinical practice, complete pain remission following SNRB indicates that the nerve root infiltrated by local anesthetics is the primary pain source.

Regrettably, prior relevant studies have demonstrated that conventional SNRB exhibits relatively low overall diagnostic accuracy, failing to achieve satisfactory sensitivity and specificity simultaneously. Uncontrolled diffusion of injectable agents is recognized as the predominant contributor to such poor diagnostic performance. Specifically, unintended anesthetic contamination of adjacent unaffected nerve roots may trigger false-positive outcomes, while insufficient delivery of local anesthetics to the targeted nerve root can result in false-negative findings. At present, no techniques or strategies for precisely regulating drug distribution during SNRB procedures have been reported in the existing literature.

Interestingly, during the nerve root fluorography in some patients in our team, when linear striation opacities are visualized within the nerve root, which indicates occurrence of intraperineural, the contrast medium typically diffuses only inside and around the targeted nerve root. This phenomenon can also be observed in the illustrative images from a previous study on therapeutic SNRB, yet it seems to have attracted little attention from researchers. Additionally, the findings of this study demonstrated that intraperineural injection occurred in approximately 30% of patients undergoing therapeutic SNRB with accidental intraperineural injection, and no cases of neurological injury were documented during follow-up. Therefore, it is reasonable to hypothesize that intraperineural injection is a safe, feasible approach that enables precise distribution of agents to the targeted nerve root.

Using the postoperative efficacy of single-segment single-nerve-root decompression as the gold standard for identifying the compressed nerve root, the present study aimed to investigate the diagnostic accuracy, safety, and technical feasibility of selective intraperineural nerve root block (SINRB) in patients with radicular pain. A double-blind approach was implemented, with participants and assessors masked to the nerve root status (responsible vs. non-responsible) during evaluations. Meanwhile, to improve the success rate of intraperineural injection, to the best of our knowledge, the present study is the first to adopt three-dimensional computed tomography multiplanar volume reconstruction (3D-CT MPVR) imaging to visualize the anatomical course of the nerve root within the intervertebral foramen.

[Sample Size Estimation] To ensure adequate statistical power for accurately evaluating the diagnostic accuracy of selective intraperineural nerve root block (SINRB) in identifying the responsible compressed nerve root (RCNR) in patients with radicular pain, sample size calculation was performed based on diagnostic test design principles, incorporating the following key parameters: (from preliminary pilot data) an expected sensitivity of 95%, specificity of 96%, 95% confidence level, ±5% margin of error, and a 10% allowance for potential missing data or patient dropout. Using the single-proportion estimation method, the required numbers of positive and negative events were calculated separately for sensitivity and specificity. The sample size required for sensitivity was 80 cases, and for specificity was 66 cases. Accordingly, we plan to enroll 66 patients with single-level lesions (anticipated to yield one positive and one negative result each) and 14 patients with multi-level lesions (anticipated to yield one positive result each). This sample size sufficiently meets the statistical power requirements for the primary study objective-evaluating the sensitivity and specificity of SINRB for RCNR identification-ensuring the scientific rigor, stability, and generalizability of the study findings.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

盲法说明

Blinding design was adopted for bias control. Both participants and independent outcome assessors remained fully blinded during diagnostic SINRB evaluation. Neither subjects nor assessors knew whether each injection targeted the suspected symptomatic responsible nerve root or a non-responsible nerve root. Participants were only informed of the predefined clinical rule: once complete pain relief was achieved following a single SINRB, subsequent blocking procedures would be discontinued. In addition, an injection may also be administered to non-responsible nerve roots to serve as a negative control, and participants would remain unaware of whether the responsible or non-responsible nerve root was injected first. Independent assessors performed clinical evaluations before and after each SINRB using separately recorded video footage. The order of video files was randomized to ensure that assessors remained unaware of how many SINRB procedures each participant had undergone.

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

研究组 & 干预措施

Preoperative Diagnostic SINRB for Responsible Compressed Nerve Root(RCNR) Localization

Experimental

All enrolled subjects will undergo the same standardized surgical procedure.

  • For patients with a single suspected lesion and RCNR (typically with ambiguous imaging findings), 2 separate SINRBs are performed (firstly at a non-responsible control root, then at the suspected RCNR) to rule out placebo effect and non-lumbar pain sources. If ≥50% pain relief occurs after the first block, the second SINRB is given the next day after local anesthetic clearance, and patients compare pain relief differences between the two sessions. If relief is less than 50%, the second SINRB is delivered after a 20-minute interval.
  • For patients with multiple nerve roots compressed, 1 SINRB is performed at the target nerve root to confirm that single-level surgical decompression can achieve complete pain relief. If complete pain relief or resolution of motor dysfunction is not achieved after the first injection, a second SINRB will be administered to an alternative suspected root to identify the true RCNR.

干预措施: Selective Intraperineural Nerve Root Block(SINRB) (Diagnostic Test)

Preoperative Diagnostic SINRB for Responsible Compressed Nerve Root(RCNR) Localization

Experimental

All enrolled subjects will undergo the same standardized surgical procedure.

  • For patients with a single suspected lesion and RCNR (typically with ambiguous imaging findings), 2 separate SINRBs are performed (firstly at a non-responsible control root, then at the suspected RCNR) to rule out placebo effect and non-lumbar pain sources. If ≥50% pain relief occurs after the first block, the second SINRB is given the next day after local anesthetic clearance, and patients compare pain relief differences between the two sessions. If relief is less than 50%, the second SINRB is delivered after a 20-minute interval.
  • For patients with multiple nerve roots compressed, 1 SINRB is performed at the target nerve root to confirm that single-level surgical decompression can achieve complete pain relief. If complete pain relief or resolution of motor dysfunction is not achieved after the first injection, a second SINRB will be administered to an alternative suspected root to identify the true RCNR.

干预措施: single-level lumbar decompression surgery (Procedure)

结局指标

主要结局

The change from baseline in standing impairment

时间窗: Baseline, 5mins after SINRB, the second day after ambulation, and 1 month postoperatively

Standing impairment was documented via separate video recordings before and after each SINRB procedure, as well as on the second day of postoperative ambulation. Upon completion of data collection, Video recordings of all participants were randomly shuffled, and independent assessors evaluated the presence or absence of standing impairment for each video. Assessors were blinded to the type of nerve root injected (responsible vs. non-responsible), final surgical outcomes, clinical information, imaging results, and the number of SINRB sessions. Video content: The patient was instructed to stand upright with chest out, head raised, and lumbar spine maintained in an extended position for 20 seconds. Assessment Criteria: Standing impairment was defined as present if the patient voluntarily bent forward/backward or left/right during the test due to intolerable radicular pain and failed to maintain the initial upright posture. Otherwise, standing impairment was considered absent.

Change from baseline in walking impairment

时间窗: Baseline, 5mins after SINRB, the second day after ambulation, and 1 month postoperatively

Walking impairment was evaluated using the same recording and blinding protocols as those for standing impairment. Video content: Patients maintained an upright position and kept uninterrupted walking for 500 meters. Judgment criteria: "walking disorder" was defined as present if voluntary termination of walking occurred before completing 500 meters due to intolerable radicular pain. Otherwise, walking impairment was considered absent.

Change from baseline in straight leg raising impairment

时间窗: Baseline, 5mins after SINRB, the second day after ambulation, and 1 month postoperatively

The straight leg raising (SLR) impairment was evaluated using the same recording and blinding protocols as those for standing impairment. Video content: The straight leg raising (SLR) test was performed sequentially on the unaffected side and the affected side. Assessment criteria: The projection of the heel of the elevated leg onto the contralateral (non-elevated) leg was used as the observation index. "Presence of SLR impairment on the affected side" was defined as: the heel projection on the affected side failing to reach the patella due to intolerable radicular pain, whereas the heel projection on the unaffected side reached the patella or cephalad to it. "Absence of SLR impairment on the affected side" was defined as: the heel projection reaching the patella at maximum SLR on the affected side, with or without tolerable radicular pain.

Subjective pain relief

时间窗: 5mins after SINRB, the second day after ambulation, and 1 month postoperatively

After each SINRB/operation, movements previously inducing severe pain (e.g., standing, walking, lying flat, stair climbing/descending) were repeated. Video questions: "Where was your worst pain during movement pre-procedure?"; "Where do you feel pain now? Point to it."; "Does residual pain affect walking speed/distance?"; "How much has pain decreased post-SINRB/surgery?" (options: no significant relief; relief with activity-limiting residual pain; essential relief \[residual pain not affecting activities\]; pain disappeared). Pain relief assessment followed the same recording and blinding protocols as for standing impairment.

次要结局

  • Result of SINRB(5mins after SINRB)
  • Overall clinical assessment after lumbar spine surgery(the second day after ambulation, and 1 month postoperatively)
  • The occurrence of complications(24hs after SINRB)
  • Changes in neurological function before and after SINRB(24hs after SINRB)
  • Success rate of SINRB procedure(immediately post-SINRB)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lingjiang Li

Attending Physician

Xi'an Honghui Hospital

研究点 (1)

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