Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Not applicable Interventional

Prometra Post-Approval Study

ClinicalTrials.gov ID: NCT01854229

Public ClinicalTrials.gov record NCT01854229. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 25, 2026, 8:09 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Non-randomized, Open-label, Multicenter Study to Evaluate the Long-term Safety of the Prometra Programmable Pump System

Study identification

NCT ID
NCT01854229
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Flowonix Medical
Industry
Enrollment
400 participants

Conditions and interventions

Interventions

  • Prometra Programmable Intrathecal Infusion Pump Device

Device

Eligibility (public fields only)

Age range
22 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 19, 2013
Primary completion
Mar 14, 2023
Completion
Mar 14, 2023
Last update posted
Oct 17, 2023

2013 – 2023

United States locations

U.S. sites
26
U.S. states
13
U.S. cities
23
Facility City State ZIP Site status
Perlman Clinic La Jolla California 92037
Pacific Pain Physicians Santa Barbara California 93105
Evolve Restorative Center Santa Barbara California 95403
Summit Pain Alliance Santa Rosa California 95401
BioHealth Pain Management Torrance California 90260
Interventional Pain Management Daytona Beach Florida 32174
Florida Institute of Medical Research Jacksonville Florida 32257
Palm Beach Pain Management Lake Worth Florida 33462
Pain Institute of Tampa Tampa Florida 33603
Global Scientific Innovations Evansville Indiana 47714
Summit Pain Management Fort Wayne Indiana 46802
Summit Research Institute Fort Wayne Indiana 46825
Interventional Pain Management Specialists Overland Park Kansas 66209
Bluegrass Pain Consultants Louisville Kentucky 40202
Kentuckiana Pain Specialists Louisville Kentucky 40241
Neuroscience and Pain Institute Covington Louisiana 70433
Integrated Pain and Neuroscience New Orleans Louisiana 70115
Jackson Anesthesia Pain Center Jackson Mississippi 39202
Triumph Medical Asheville North Carolina 28803
Integrated Pain Solutions Columbus Ohio 43219-1531
Pain Management Institute Wooster Ohio 44691
Neurospine Institute Eugene Oregon 97401
Pain Care of Oregon Medford Oregon 97504
Fox Chase Pain Management Associates Trevose Pennsylvania 19053
Space City Pain Specialists Webster Texas 77598
Nexus Pain Care Provo Utah 84604

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01854229, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 17, 2023 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01854229 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →