Cryolesion in Treatment of Phantom Limb Pain

Status Recruiting

Clinical Trial Summary

Assessment of pain intensity on the NRS. Assessment of the quality of life by SF-36 and AIS. Diagnostic/prognostic nerve block with 5 ml of 2% lidocaine under real-time ultrasound control with confirmation of the correct position of the needle using a peripheral nerve stimulator.

Reassessment of pain intensity on the NRS 30 minutes after local anesthetic block.

Cryoablation under real-time ultrasound control if the NRS value is reduced by ≥ 2 points.

If pain intensity on the NRS reduced by less than 2 points, reassessment 60 minutes after local anesthetic block.

Cryoablation under real-time ultrasound control if the NRS value is reduced by ≥ 2 points.

If pain intensity on the NRS reduces by less than 2 points 60 minutes after local anesthetic block cryoablation will not be performed.

Cryoablation effect will be evaluated 24 hours, 7 days, 30 days, 3 months, 6 months post procedure.

- 24 hours after the procedure - assessment of pain intensity and quality of life

- 7 days after the procedure - assessment of pain intensity

- 30 days after the procedure - assessment of pain intensity and quality of life

- 3 months after the procedure - assessment of pain intensity

- 6 months after the procedure - assessment of pain intensity and quality of

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03415360
Study type	Interventional
Source	Military Institute of Medicine, Poland
Contact	Dariusz Tomaszewski, MD PhD
Phone	00 48501 190 386
Email	dtomaszewski@wim.mil.pl
Status	Recruiting
Phase	N/A
Start date	February 9, 2018
Completion date	January 2020

View Details

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