At a glance
ClinicalIndex Comparison RecordN/ACompleted· 10 enrolled
Drug / intervention
Peripheral Nerve Stimulationdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Investigational Device Exemption for Intrathoracic Nerve Stimulation
In Brief
A clinical study evaluating Peripheral Nerve Stimulation for Postoperative Pain. Completed, enrolled 10 participants across 1 site.
Detailed Summary
The purpose of this study is to conduct an early clinical evaluation of safety and feasibility of peripheral nerve stimulation (PNS) of the intercostal nerves using an electrical lead placed in the thoracic cavity as a safe and effective method of pain control after cardiothoracic surgery.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPostoperative Pain
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
Enrollment StartAug 2019
First PostedAug 2019
Primary CompletionJan 2024
Study CompletionJun 2024
TodayJul 2026
First PostedAug 26, 2019
Enrollment StartAug 13, 2019
Primary CompletionJan 9, 2024
Study CompletionJun 11, 2024
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 6.9 years ago
Interventions
Peripheral Nerve Stimulationdevice
Medtronic Intellis Spinal Cord Stimulation Device to be implanted in thoracic cavity to treat postoperative acute pain.