Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity
NCT: NCT06340451 · RECRUITING
Brief Summary
This multicenter, randomized, double-blind, sham-controlled study is designed to evaluate the efficacy and safety of the iovera° system in subjects with upper extremity spasticity. A total of approximately 132 subjects will be enrolled; 88 subjects will receive treatment with the iovera° system and 44 subjects will receive sham treatment (sham iovera° system treatment).
Frequently Asked Questions
What is Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity?
Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity is a clinical trial registered under NCT06340451. Current status: RECRUITING.
What is the status of NCT06340451?
The current status of NCT06340451 (Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity) is: RECRUITING.
When did Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity start?
Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity started on 2024-07-11.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.