At a glance
ClinicalIndex Comparison RecordN/ACompleted· 110 enrolled
Drug / intervention
Infusion Pump (Prometra)device
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.
Prometra's Utilization in Mitigating Pain (PUMP)
In Brief
A clinical study evaluating Infusion Pump (Prometra) for Intractable Pain. Completed, enrolled 110 participants across 3 sites.
Detailed Summary
Clinical evaluation of the safety and efficacy of the Prometra Programmable Infusion Pump to accurately supply drug to the intrathecal space for the treatment of chronic pain.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIntractable Pain
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartJan 2007
Primary CompletionMar 2008
First PostedJan 2009
Study CompletionMar 2011
TodayJul 2026
First PostedJan 6, 2009
Enrollment StartJan 1, 2007
Primary CompletionMar 1, 2008
Study CompletionMar 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 17.5 years ago
Interventions
Infusion Pump (Prometra)device
Implantation of pump/catheter for infusion of morphine into the intrathecal space