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UnknownNCT03415360

Cryolesion in Treatment of Phantom Limb Pain

Percutaneous Cryoablation in the Treatment of Neuropathic Pain Post Limb Amputation

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Military Institute od Medicine National Research Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
PROCEDUREcryoablationcryoablation of nerve responsible for phantom limb pain

Timeline

Start date
2018-02-09
Primary completion
2019-06-01
Completion
2020-01-01
First posted
2018-01-30
Last updated
2018-09-25

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT03415360. Inclusion in this directory is not an endorsement.