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Completed No phase listed Observational

A Prospective Clinical Outcomes Registry

ClinicalTrials.gov ID: NCT01305525

Public ClinicalTrials.gov record NCT01305525. 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 Sep 12, 2026, 8:22 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

Partnership for Advancement In Neuromodulation (PAIN): A Prospective Clinical Outcomes Registry

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective non-interventional 24 month post implant registry. Any patient that receives a St. Jude Medical FDA approved implantable neuromodulation system is eligible for enrollment. A minimum of 600 patients will be enrolled from a minimum of 30 sites. Patients will be enrolled post-implant and followed for 24 months. Data are collected at enrollment (within 30 days of device implant), and routine care follow-up visits at 3 months, 6 months, 12 months, 18 months and 24 months.

Study identification

NCT ID
NCT01305525
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Abbott Medical Devices
Industry
Enrollment
614 participants

Conditions and interventions

Conditions

Eligibility (public fields only)

Age range
18 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
May 31, 2009
Primary completion
Mar 31, 2014
Completion
Mar 31, 2014
Last update posted
Jan 29, 2019

2009 – 2014

United States locations

U.S. sites
31
U.S. states
18
U.S. cities
31
Facility City State ZIP Site status
Not listed Scottsdale Arizona
Not listed Azusa California
Not listed Chula Vista California
Not listed Sacramento California
Not listed Jacksonville Florida
Not listed Tampa Florida
Not listed Evansville Indiana
Not listed Muncie Indiana
Not listed Louisville Kentucky
Not listed Baton Rouge Louisiana
Not listed Bloomfield Hills Michigan
Not listed Waterford Michigan
Not listed Saint Paul Minnesota
Not listed Kalispell Montana
Not listed New York New York
Not listed Syracuse New York
Not listed Utica New York
Not listed Williamsville New York
Not listed Durham North Carolina
Not listed Winston-Salem North Carolina
Not listed Mansfield Ohio
Not listed Purcell Oklahoma
Not listed Bethlehem Pennsylvania
Not listed Houston Texas
Not listed Southlake Texas
Not listed Webster Texas
Not listed Arlington Virginia
Not listed Edmonds Washington
Not listed Kirkland Washington
Not listed Charleston West Virginia
Not listed Morgantown West Virginia

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01305525, 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 Jan 29, 2019 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01305525 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →