Viewing Study NCT06467669



Ignite Creation Date: 2024-07-17 @ 11:19 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06467669
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-21
First Post: 2024-06-07

Brief Title: Predictive Outcomes for Selective Thumb Carpometacarpal Joint Denervation
Sponsor: University of Calgary
Organization: University of Calgary

Study Overview

Official Title: Predictive Outcomes for Selective Thumb Carpometacarpal Joint Denervation
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Background The thumb or first carpometacarpal CMC joint is commonly affected by osteoarthritis Literature has reported a prevalence of 15 in women and 7 in men First CMC joint osteoarthritis can present with decreased grip strength pain instability and inability to engage in routine daily activities Definitive management is with surgery however these are associated with known risks and increased weight times for the patient First CMC joint denervation surgery is supported in the literature as a safe and effective approach to treat pain strength and thumb opposition which still allows for definitive surgery to be performed later if the arthritis progressed or if the pain returned later after the surgery

Objectives 1 evaluate the effectiveness of the neurectomy in patients with with CMC arthritis with respect to pain relief functional parameters and Quick disabilities of the arm shoulder and hand QuickDASH scores 2 to determine whether pain relief with selective nerve blocks are predictive of the outcome of the combined neurectomy and 3 to determine whether improvement in grip strength following selective blocks is predictive of final grip strength and outcome following neurectomy

Methods Patients referred to the plastic surgery clinic for assessment of symptomatic first CMC joint osteoarthritis will be provided options for standard treatment or denervation procedure Patients who agree to denervation will undergo local anesthetic block at their initial consult At their initial consultation as well as at the 2-week 3-month 6-month 12-month and 24-month post-surgical follow-up patients will complete a QuickDASH Kapandji score pain scores 2-point discrimination and gripkey3-point strength measurements The total patient population included in this study will be 60 patients
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None