Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06635200
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-10-08
Brief Title:
Pain Phenotype in Patients With Carpal Tunnel Syndrome
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Determination of Dominant Pain Phenotype in Patients With Carpal Tunnel Syndrome
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of this study was to determine the dominant pain phenotype in a group of patients with Carpal Tunnel Syndrome by applying the International Association for the Study of Pain IASP criteria
Detailed Description:
Voluntary participants between the ages of 18-65 who have been diagnosed with CTS will be included in the studyThe 7 steps in the Clinical CriteriaRating System determined by the International Association for the Study of Pain IASP for Nosiplastic Pain and Carpal Tunnel Syndrome will be applied to people with CTS Pressure pain threshold thermal pain threshold mechanical pain sensitivity and allodynia will be evaluated to determine pain hypersensitivity Step 5 Specific questions will be asked to confirm the history of hypersensitivity in patients Step 6 Finally comorbidities if any will be determined Step 7 As a result the pain phenotype of patients with CTS will be determined Nociceptive Neuropathic or Nosiplastic Shapiro-Wilk test will be performed to determine the distribution of the data One-way ANOVA continuous or Kruskal-Wallis categorical will be used to examine whether the dependent variables differ between groups For significant F-test an additional investigation of differences between groups will be performed with Gabriels post hoc procedure
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None