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RecruitingNCT07113184ClinicalTrials.gov record

Randomized a Clinical Trial With Medical Device in Acute Ischemic Stroke

Acute Ischemic Stroke

THE QUICK READ

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
Understand screening

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

Prepare your questions

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.

No results are flagged as posted.

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
María Teresa Díaz MartíCONTACTtdmarti@hotmail.com
View location on map ↗
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

A HUMAN NEXT STEP

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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