Randomized a Clinical Trial With Medical Device in Acute Ischemic Stroke
Acute Ischemic Stroke
What this study involves
The registry says this study is recruiting. Individual locations may have different availability.
- Study type
- Interventional
- Phase
- Not applicable
- Age range
- 18 years - Not specified
- Sex eligible
- All sexes
- Healthy volunteers
- Not accepted
- Participants
- 220 Estimated
These are starting points, not an eligibility decision. The research team must review the full requirements.
About the research
This study seeks to provide high-quality evidence on the potential benefits of the dual stentriever approach, potentially informing future clinical guidelines and improving outcomes in patients with anterior circulation large vessel occlusion strokes.
Who may be able to participate?
The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.
Inclusion Criteria:
- Age ≥ 18
- NIHSS ≥ 6
- mRS ≤ 1
- Proximal anterior circulation occlusion
- ASPECTS \> 6
- Informed consent
Exclusion Criteria:
- Absence of occlusion
- Posterior circulation stroke
- Carotid dissection or tandem stenosis requiring treatment
- Severe comorbidities or contraindications to imaging contrast
Treatment, groups and participation
The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.
- Assignment
- Random assignment
- Masking
- Single masked
Dual Stentriever
Endovascular mechanical thrombectomy with dual or stentriever technique using a balloon guiding catheter.
Device: dual sr
Single Stentriever
Endovascular mechanical thrombectomy with single stentriever technique using a balloon guiding catheter.
Device: single sr
dual sr DEVICE
Dual Stentriever
single sr DEVICE
Single Stentriever
What researchers are measuring
Outcome measures describe what is being studied. They are not proof that a treatment works.
Primary measures
Time takes in achieving complete reperfusion after a single thrombectomy pass.
Time frame: 24 hours or 48 hours after thrombectomy
To evaluate the superiority of the dual stentriever technique in achieving complete reperfusion after a single thrombectomy pass.
Review the complete result tables and limitations in the official record.
Open official results ↗Research locations (4)
The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.
4 locations
Hospital de BurgosBurgos, SpainRecruiting
Hospital Regional de MálagaMálaga, SpainRecruiting
Complejo Hospitalario de SalamancaSalamanca, SpainRecruiting
Hospital universitario marques de valdecillaSantander, SpainRecruiting
Study team and timeline
- Lead sponsor
- Instituto de Investigación Marqués de Valdecilla
- Study start
- Mar 1, 2026 Actual
- Primary completion
- Mar 1, 2027 Estimated
- Study completion
- Dec 31, 2027 Estimated
- First posted
- Aug 8, 2025 Actual
- Last updated
- Nov 10, 2026 Actual
Official study contacts
No central contact is listed. Check the locations and the official record.
Official study title
DUAL VERSUS SINGLE STENTRIEVER FOR RECANALIZATION IN ACUTE ISCHEMIC STROKE: THE RANDOMIZED DOUBLE UP TRIAL
Ask Wellness Clinical Research
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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.
Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026
