drugset / Trial / NCT06919289

The Investigators Are Comparing Lidocaine and Papaverine Nerve Blocks to Determine Which Improves Blood Flow Better, Making the "Phoenix Sign" Clearer on Imaging. This Helps Accurately Diagnose Nerve Compression, Improving Patient Care

NCT06919289

Completed 4 enrolled US Neuropathy Centers
RandomizedCrossoverDouble-blindDiagnostic

Summary

This pilot study aims to investigate the effects of nerve blocks in patients with diabetic peripheral neuropathy through a double-blinded, randomized trial involving 4 patients. Each participant will receive bilateral peripheral nerve blocks using either lidocaine or papaverine. Following randomization, each patient will receive one medication in one leg and the alternate medication in the contralateral leg. Researchers will measure parameters including motor strength, sensory function (two-point discrimination), arterial blood flow via Doppler ultrasound, and microvascular perfusion using near-infrared spectroscopy both prior to and following nerve block administration. This research seeks to explore potential diagnostic and therapeutic applications for peripheral nerve entrapment, a common yet challenging clinical condition.

Timeline

Start
2024-03-07
Primary completion
2024-03-07
Completion
2024-07-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lidocaine Other / unclassified 0.5 ml Other
Comparator Papaverine Small molecule 15 mg Other

Indications