RECRUITING

SuperSaturated Oxygen Comprehensive Observational Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The SuperSaturated Oxygen Comprehensive Observational Registry (SSCORE) registry, a prospectively designed observational study, aims to evaluate the clinical utility and effectiveness of SuperSaturated Oxygen (SSO2) Therapy versus percutaneous coronary intervention (PCI) alone among patients with anterior acute myocardial infarction (AMI) in routine clinical practice. The goal is to collect real-world data from patients treated with SSO2 Therapy to determine its impact on the overall heart failure (HF) burden on patients and healthcare systems compared with usual care for treatment of patients with AMI. The SSCORE Registry will generate effectiveness and healthcare resource utilization data that will be used in cost-effectiveness analysis modeling.

Official Title

SuperSaturated Oxygen Comprehensive Observational Registry

Quick Facts

Study Start:2024-08-13
Study Completion:2029-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06438315

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Jennifer Gardner
CONTACT
949-300-2811
sscore.zoll@zoll.com

Principal Investigator

William W O'Neill, MD
PRINCIPAL_INVESTIGATOR
Henry Ford Hospital

Study Locations (Sites)

Carle Health Methodist Hospital
Peoria, Illinois, 61636
United States
Abbott Northwestern Hospital
Minneapolis, Minnesota, 55407
United States
United Hospital
Saint Paul, Minnesota, 55102
United States
North Shore University Hospital
Manhasset, New York, 11030
United States
Long Island Jewish Hospital
Queens, New York, 11040
United States
St Mary's Medical Center
Huntington, West Virginia, 25702
United States

Collaborators and Investigators

Sponsor: TherOx

  • William W O'Neill, MD, PRINCIPAL_INVESTIGATOR, Henry Ford Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-08-13
Study Completion Date2029-03-31

Study Record Updates

Study Start Date2024-08-13
Study Completion Date2029-03-31

Terms related to this study

Additional Relevant MeSH Terms

  • STEMI - ST Elevation Myocardial Infarction
  • AMI