RECRUITING

Balloon Guide Versus Conventional Guide Catheter in Stroke Thrombectomy

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 purpose of this clinical trial is to study the two main types of approaches used in stroke thrombectomy and to investigate if one approach is more effective than the other, as this is currently not known. This study will be conducted in adults who have been diagnosed with an acute ischemic stroke and who are undergoing a thrombectomy for the treatment of their stroke. The main questions it aims to answer are: * Does the use of a balloon guide catheter versus a conventional guide catheter lower the time needed to restore blood flow in the blocked vessel in the brain * To help researchers better understand the technical, clinical, and procedural outcomes associated with using a balloon guide catheter versus a conventional guide catheter in stroke thrombectomy Participants will be asked to * Share their medical history and imaging data that is collected as part of their routine medical care * Undergo a mechanical thrombectomy as part of their routine medical care * Answer some questions about their neurological functioning at 3 months (90 days) post hospitalization

Official Title

Balloon Guide Versus Conventional Guide Catheter in Stroke Thrombectomy

Quick Facts

Study Start:2025-07
Study Completion:2028-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07085390

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. * Patient is undergoing a stroke thrombectomy procedure at the enrolling hospital
  3. * Patient or the legally authorized representative are able to provide signed informed cosent for the study
  4. * Patient is not enrolled in another clinical trial that may interfere with the results or interpretation of this study
  5. * Identification of a Large Vessel Occlusion (LVO) on imaging
  1. * Lack of signed informed consent from the patient or legally authorized representative
  2. * Spontanous recanalization or any other reason in which the mechanical thrombectomy procedure would be terminated

Contacts and Locations

Study Locations (Sites)

University of South Florida (USF)
Tampa, Florida, 33606
United States

Collaborators and Investigators

Sponsor: University of South Florida

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 Date2025-07
Study Completion Date2028-07

Study Record Updates

Study Start Date2025-07
Study Completion Date2028-07

Terms related to this study

Keywords Provided by Researchers

  • Ischemic Stroke
  • Thrombectomy

Additional Relevant MeSH Terms

  • Acute Ischemic Stroke AIS