Found 16 matching trials
Prometra Post-Approval Study NA The Prometra Pump is approved by the FDA for use in the United States. The ...
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Patient Preference and Long-term Outcomes in Persistent Spinal Pain Syndrome: A Prospective Study Comparing Spinal Cord Stimulation to Intrathecal Drug Delivery. PHASE4 Spinal cord stimulation (SCS) or intrathecal drug delivery (pain pump) can ...
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University Hospitals Cleveland Medical Center
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The Clinical Evaluation of Implantable Pump System For Safety And Delivery Accuracy In Patients Requiring Intrathecal Administration Of Morphine Sulfate For Chronic Pain PHASE2 • The objectives of this study are to confirm the medication delivery accur...
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Center for Pain & Supportive Care
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A Pilot Study to Evaluate the Efficacy of ITDD vs. CMM in the Treatment of Pancreatic Cancer Pain NA The purpose of this study is to compare efficacy of pain treatment with ITD...
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Menorah Medical Center
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Single-arm Study to Assess the Safety of Hydromorphone Hydrochloride by Intrathecal Administration PHASE3 The purpose of this study is to evaluate the long-term safety of hydromorph...
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The Center for Clinical Research
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Intrathecal Morphine Administration Using Implantable Pump With Continuous or Programmable Flow NA The aim of this study is to compare intrathecal morphine administration: us...
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Implantable System for Remodulin Post-Approval Study N/A The purpose of the Implantable System for Remodulin (ISR) Post Approval Stu...
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Multiple Locations
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Prometra's Utilization in Mitigating Pain II N/A Intrathecal infusion pumps are increasingly used to deliver analgesics for ...
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Approved For Marketing
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Multiple Locations
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Long-term Surveillance of the MedStream Programmable Infusion System N/A This post-approval study will primarily evaluate the long-term safety of th...
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UMass Memorial Medical Center
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Safety and Efficacy Study of Hydromorphone Hydrochloride by Intrathecal Administration PHASE3 The purpose of this study is to determine the safety and efficacy of hydrom...
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The Center for Clinical Research
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