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A Non-invasive Intervention (BreEStim) for Management of Phantom Limb Pain (PLP) After Limb Amputation (Experiment 3)

Pain Management Clinical Trial

Official title:
A Non-invasive Intervention (BreEStim) for Management of Phantom Limb Pain (PLP) After Limb Amputation (Experiment 3)

Clinical Trial Summary

The purpose of this study is to compare the effectiveness of innovative intervention of breathing controlled electrical stimulation (BreEStim) and conventional electrical stimulation (EStim) in management of neuropathic phantom limb pain in patients after limb amputation after multiple sessions of treatment.

Clinical Trial Description

Subjects will receive 10-session BreEStim and 10-session EStim treatment in a random order. The interval between BreEStim and EStim is at least 2 weeks. The following assessment will be made before and after 1. Visual analogue scale (VAS). 2. Quantitative sensory testing (QST). It includes non-invasive assessment of tactile sensation threshold (TST), electrical sensation threshold (EST), electrical pain threshold (EPT), and thermal thresholds. 3. Hear rate variability (HRV). It consists of 5-minute electrocardiogram (ECG) recording before and after a treatment session. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04751526
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact Sheng Li, MD, PhD
Phone (713) 797-7125
Email sheng.li@uth.tmc.edu
Status Recruiting
Phase N/A
Start date April 2, 2021
Completion date August 31, 2024
View Details
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