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Completed No phase listed Observational Results available

Postmarket Outcomes Study for Evaluation of the Superion™ Spacer

ClinicalTrials.gov ID: NCT04563793

Public ClinicalTrials.gov record NCT04563793. 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 Nov 3, 2026, 9:29 PM EST

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

Brief summary

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

To compile real-world outcomes of the Superion™ IDS in routine clinical practice.

Study identification

NCT ID
NCT04563793
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Boston Scientific Corporation
Industry
Enrollment
129 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
21 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
Oct 8, 2020 (Actual)
Primary completion
Mar 20, 2023 (Actual)
Completion
Mar 20, 2023 (Actual)
Last update posted
Jan 13, 2025

2020 – 2023

United States locations

U.S. sites
23
U.S. states
12
U.S. cities
23
Facility City State ZIP Site status
Pain Medicine Associates Fountain Valley California 92708 —
California Orthopedics & Spine Larkspur California 94939 —
Relieve Pain Center, Inc. San Diego California 92103 —
Source Healthcare Santa Monica California 90403 —
Pacific Research Institute Santa Rosa California 95403 —
IPM Medical Group Inc Walnut Creek California 94598 —
Holy Cross Hospital Inc. Fort Lauderdale Florida 33308 —
Louis J. Raso, MD, PA Jupiter Florida 33477 —
Florida Pain Institute Merritt Island Florida 32953 —
Southwest Florida Pain Center Port Charlotte Florida 33948 —
Georgia Pain and Spine Care, Inc. Newnan Georgia 30265 —
Centurion Spine and Pain Centers Waycross Georgia 31501 —
North Idaho Day Surgery LLC Post Falls Idaho 83854 —
Rush University Medical Center Chicago Illinois 60612 —
University of Kansas Hospital Kansas City Kansas 66160 —
KC Pain Centers Lee's Summit Missouri 64086 —
Comprehensive and Interventional Pain Management LLP Henderson Nevada 89052 —
Premier Pain Center Shrewsbury New Jersey 07702 —
University Clinical Research Center Somerset New Jersey 08873 —
The Toledo Clinic Toledo Ohio 43623 —
Center for Interventional Pain and Spine Bryn Mawr Pennsylvania 19010 —
Advanced Spine Pain Solution Laredo Texas 78041 —
Precision Spine Care Tyler Texas 75701 —

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 NCT04563793, 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 13, 2025 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04563793 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →