LivaNova PLC ((LIVN)) announced an update on their ongoing clinical study.
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Study Overview: LivaNova PLC is conducting a study titled A Prospective, Multi-center, Randomized Controlled Blinded Trial Demonstrating the Safety and Effectiveness of VNS Therapy® System as Adjunctive Therapy Versus a No Stimulation Control in Subjects With Treatment-Resistant Depression. The study aims to evaluate whether active Vagus Nerve Stimulation (VNS) Therapy is more effective than no stimulation in reducing depressive symptoms in patients with treatment-resistant depression over a 12-month period.
Intervention/Treatment: The intervention being tested is the Vagus Nerve Stimulation (VNS) device, an implantable device designed to stimulate the vagal nerve. The study compares active VNS therapy to a control group with no stimulation for the first 12 months.
Study Design: This is a randomized, controlled, and quadruple-blinded trial with a parallel intervention model. Participants, care providers, investigators, and outcomes assessors are blinded. The primary purpose of the study is treatment-focused, with a 1:1 randomization between active stimulation and no stimulation groups.
Study Timeline: The study began on March 21, 2019, and is currently recruiting. The primary completion and estimated completion dates are not specified, but the last update was submitted on July 24, 2025. These dates are crucial for tracking the study’s progress and anticipated results.
Market Implications: The ongoing study could significantly impact LivaNova’s stock performance and investor sentiment, especially if the results demonstrate the effectiveness of VNS therapy in treating depression. Success in this trial may position LivaNova favorably against competitors in the medical device industry, potentially leading to increased market share and revenue.
The study is ongoing, with further details available on the ClinicalTrials portal.
