Catheter-Based Sacral Nerve Block Versus Pudendal Nerve Block in the Treatment of Pudendal Neuralgia: A Randomized Double-Blinded Controlled Trial
In brief
Sacral nerve block doubles sitting time and lowers pain versus pudendal block
In a randomized trial of 90 refractory pudendal neuralgia patients, daily catheter-based sacral nerve block reduced visual analogue pain scores by about one point and increased maximum sitting tolerance to roughly 69 minutes, versus 38 minutes with pudendal block, over six months. The approach was well tolerated, but larger studies are needed to confirm safety and feasibility.
- Journal
- European journal of pain (London, England) (Q1)
- Published
- 1 August 2026
- Study design
- Randomized controlled trial
- Evidence level
- Level 1, High (CEBM 1b)
- Authors
- Kai-Kai Guo, Jing Li, Ying Meng, Long Wang, Shu-Rong Li, Gui-Jun Lu, et al.
- PMID
- 42559665
- DOI
- 10.1002/ejp.70355
Why clinicians should know about it
- Picked for Anesthesiology and Pain Medicine (top studies of the week, 9 August 2026).
- Picked for Radiology, Radiation Oncology, Nuclear Medicine, Medical Physics and Imaging (top studies of the week, 9 August 2026): Phase 3 RCT of catheter-based sacral vs pudendal nerve block
- Picked for Geriatrics and Gerontology (top studies of the week, 9 August 2026).
- Picked for Infectious Diseases (top studies of the week, 9 August 2026).
- Picked for Health Policy (top studies of the week, 9 August 2026).
- Picked for Neurosurgery (top studies of the week, 9 August 2026).
Abstract
BACKGROUND: Pudendal neuralgia (PN) severely impacts quality of life, particularly sitting. Uncertainty exists whether catheter-based sacral nerve block with daily intermittent bolus (SNB) or pudendal nerve block (PNB) is more effective. This trial compared their efficacy over 6 months. METHODS: A prospective, randomized, double-blinded trial in China enrolled 90 PN patients. Patients were randomized to CT-guided catheter-based PNB near the pudendal nerve or SNB through the third posterior sacral foramen. In both groups, the catheter remained in place for 7 days, and 10 mL of 0.2% ropivacaine was administered once daily as an intermittent bolus, with compound betamethasone administered on Day 7. Primary outcome was pain intensity (VAS) over 6 months; secondary outcomes included patient-reported global outcomes and maximum sitting time at 6 months. RESULTS: The SNB group had significantly lower VAS scores at 1 month (2.98 ± 1.47 vs. 3.72 ± 1.08, p = 0.04), 3 months (3.36 ± 1.14 vs. 4.17 ± 1.19, p = 0.02), and 6 months (3.85 ± 1.04 vs. 4.95 ± 1.08, p < 0.0001). Significantly more SNB patients reported excellent/good outcomes at 1 month (83.88% vs. 63.40%, p = 0.04) and 6 months (75.61% vs. 37.50%, p = 0.002). Maximum sitting time at 6 months was longer with SNB (68.56 ± 21.61 vs. 37.65 ± 16.25 min, p < 0.0001). No severe complications occurred. CONCLUSIONS: SNB provided superior and sustained pain relief, functional improvement, and patient satisfaction compared to PNB over 6 months in PN patients. Broader sacral root (S2-4) coverage by SNB may enhance efficacy by targeting pudendal neuropathy and central sensitization. SNB may be considered as an intermediate minimally invasive option for selected refractory PN patients in experienced centers, pending larger safety and feasibility studies. SIGNIFICANCE STATEMENT: This first RCT directly comparing catheter-based nerve blocks for pudendal neuralgia demonstrates that sacral nerve block (SNB targeting S2-4) provides significantly superior and sustained pain relief, functional gains (doubled sitting tolerance), and patient satisfaction over pudendal nerve block (PNB) at 6 months. Its broader root coverage likely addresses central sensitization alongside neuropathy. Catheter-based sacral nerve block with daily intermittent bolus may represent an intermediate minimally invasive option for selected patients with refractory PN in experienced centers capable of structured catheter monitoring. Because this trial was not powered to estimate rare infectious complications and required a 7-day inpatient protocol, larger multicenter studies are needed to define safety, feasibility, cost-effectiveness, and the potential for outpatient adaptation.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.