Actively Recruiting
Effectiveness of Desensitisation and Pain Neuroscience Education in Patients With Carpal Tunnel Syndrome With Nosiplastic Pain
Led by Kutahya Health Sciences University · Updated on 2025-08-12
40
Participants Needed
1
Research Sites
136 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of our study was to determine the effectiveness of desensitisation and pain neuroscience education in a group of patients with mixed phenotype pain (neuropathic and nosiplastic).
CONDITIONS
Official Title
Effectiveness of Desensitisation and Pain Neuroscience Education in Patients With Carpal Tunnel Syndrome With Nosiplastic Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with Carpal Tunnel Syndrome
- Suitable for the nosiplastic pain phenotype
- Aged between 18 and 65 years
- Volunteered to participate in the study
You will not qualify if you...
- Having systemic inflammatory disease
- Having a disease that may cause polyneuropathy such as diabetes mellitus
- Having a pacemaker
- Having a disease affecting the central nervous system
- Having cervical radiculopathy
- History of previous operation or local steroid injection due to Carpal Tunnel Syndrome
- Hypersensitivity to heat and cold
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kutahya Health Science University
Kütahya, Turkey (Türkiye)
Actively Recruiting
Research Team
E
Emrah Afsar, Phd
CONTACT
A
Ayse Kocak Sezgin, Phd
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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