NCT07478042Completed
Guiding Catheters in Endovascular Stroke Therapy - Are Balloon Guided Catheters Superior?
Sind Ballonassistierte Führungskatheter in Der Endovaskulären Schlaganfalltherapie Der Vorderen Zirkulation überlegen? (BEST-Studie) Guiding Catheters in Endovascular Stroke Therapy - Are Balloon Guided Catheters Superior?
Source: ClinicalTrials.gov · Last updated 17 Mar 2026
Brief summary (registry, in English)
The BEST study is an academically initiated, single-center, prospective, randomized controlled clinical trial investigating the potential advantages and disadvantages of using a guide catheter with or without a balloon in the interventional treatment of acute ischemic stroke. The study population consists of adult patients with acute ischemic stroke of the anterior circulation for whom interventional recanalization therapy via catheter is indicated following interdisciplinary consultation between the Department of Neurology and Neuroradiology at Heidelberg University Hospital. In addition to routine clinical treatment measures and data collection, patients will be interviewed by telephone after 90 days to assess their quality of life and level of independence using standardized scoring systems. All medical devices used or investigated in this study bear the CE mark (Conformité Européenne ) and will be used within their intended purpose. Study participants will not be subjected to any additional invasive or burdensome procedures beyond normal usage.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 110 (actual)
- First submitted
- 10 Feb 2026
- Start date
- 15 Mar 2023
- Primary completion date
- 30 Jul 2025
- Lead sponsor
- University Hospital Heidelberg
- Diseases
- Stroke
- NCT number
- NCT07478042
What you commit to
- Study type: Interventional
- Participants enrolled: 110
- From 15 Mar 2023 to the primary completion date, 30 Jul 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with contraindications to interventional therapy
Other illness
- Patients with acute intracranial hemorrhage
- National Institute of Health Stroke Scale (NIHSS) ≤ 4
Other
- Pregnancy/Breastfeeding
- Pre-therapeutic mRS \> 3
- Patients detained in an institution by court or government order
- Patients who require intubation for treatment
Who the study is looking for
- Patients with an acute ischemic stroke
- Location of the primary occlusion in the anterior cerebral circulation
- Pre-therapeutic modified Rankin Scale (mRS) score of ≤ 3.
- Written informed consent from
- the patient or
- their legal representative/guardian or
- patient enrollment by an independent physician and the principal investigator
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital Heidelberg Coordinator of this site? Confirm its status | Heidelberg | Germany | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.