Last updated: October 26, 2023
Sponsor: Maxima Medical Center
Overall Status: Active - Recruiting
Phase
N/A
Condition
Peripheral Neuropathy
Fibromyalgia
Chronic Pain
Treatment
Sodium channel mutation
Clinical Study ID
NCT05877274
NL84021.015.23
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria: In order to be eligible to participate in this study, a subject must be diagnosed withACNES and receive treatment at our outpatient clinic. Additionally, subject has to meet oneof the following criteria:
- Known to have a first- or second-degree relative with ACNES;
- Have more than one recurrence of ACNES after a pain free period or ACNES at multiplelocations in the abdominal wall;
- Persistent pain after posterior neurectomy.
Exclusion
Exclusion Criteria:
- Inability to understand Dutch language.
- Known neuromuscular or neurodegenerative disease.
Study Design
Total Participants: 50
Treatment Group(s): 1
Primary Treatment: Sodium channel mutation
Phase:
Study Start date:
October 03, 2023
Estimated Completion Date:
December 31, 2024
Connect with a study center
Maxima Medical Center
Veldhoven, 5504 DB
NetherlandsActive - Recruiting
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