Last updated: September 28, 2023
Sponsor: Vancouver Island Health Authority
Overall Status: Active - Recruiting
Phase
N/A
Condition
Limb Spasticity
Treatment
N/AClinical Study ID
NCT06051656
H22-03181
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Adult patients(at least 18 years old).
- Severe claw hand with less than 4 cm distance between the pulp of the fingers and palmof the hand.
- MAS>= 3 in wrist and hand muscles interfering with function or causing a clinicalproblem, due to any neurological condition.
- Have refractory pain in wrist and hand areas with no response to the usual painmanagement methods including oral medication or botulinum toxin injection.
- Patients are already candidate for cryoneurolysis to manage the pain and spasticity intheir hand and wrist, based on their response to diagnostic nerve block test (DNB).
- Ability to attend testing sessions, comply with testing protocols and provide writteninformed consent. For patients who physically are not able to complete the consentprocess, a witness may be asked to sign and confirm their willing for participation.Legal representative may be asked to help with consent process for participants whocognitively are not able to consent on their behalf.
Exclusion
Exclusion Criteria:
- Have undergone any previous peripheral nerve procedures in their affected side, forthe treatment of spasticity, including previous cryoneurolysis, chemical neurolysis,neurectomy or arthroplasty.
- Patients who received botulinum toxin in past 4 months in the same targeted musclesfor cryoneurolysis, however, they may enter the study at the 4-month mark.
Study Design
Total Participants: 25
Study Start date:
January 09, 2023
Estimated Completion Date:
September 30, 2024
Study Description
Connect with a study center
Victoria General Hospital
Victoria, British Columbia V8Z 6R5
CanadaActive - Recruiting
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