Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05230914

A Randomized Trial of Imaging Selection Modalities for Stroke Thrombectomy (NO-SELECT)

Led by Xinqiao Hospital of Chongqing · Updated on 2025-12-26

1846

Participants Needed

8

Research Sites

150 weeks

Total Duration

On this page

Sponsors

X

Xinqiao Hospital of Chongqing

Lead Sponsor

T

The First Affiliated Hospital of Hainan Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Several studies suggest that advanced multi-modal imaging with CTP should be used to screen late time window stroke patients for thrombectomy. However, NCCT is more accessible when comparing with CTP. It is unclear whether the NCCT-based ASPECTS can be used as an imaging criterion to screen patients for thrombectomy. The newly published MR CLEAN-LATE and TENSION trials used NCCT or CTA, but still relied on ASPECTS scores to evaluate and select patients for endovascular therapy. However, different trials have different time windows. The aim of this trial was to assess the clinical outcomes of stroke patients with anterior large vessel occlusion who selected by simple imaging (NCCT) comparing via standard imaging screening strategy (CTP/MRI). The hypothesis is that simple imaging is non-inferior to standard imaging selection strategy in terms of achieving favorable outcomes.

CONDITIONS

Official Title

A Randomized Trial of Imaging Selection Modalities for Stroke Thrombectomy (NO-SELECT)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years or older
  • Last known well to hospital arrival within 24 hours
  • Acute stroke confirmed by symptoms or imaging
  • FAST ED score of 4 or higher
  • Written informed consent from patient or legal representative
Not Eligible

You will not qualify if you...

  • Allergy to radiographic contrast agents or nitinol devices
  • Currently pregnant or lactating (women patients)
  • Arterial tortuosity or disease preventing device reach
  • Preexisting neurological or psychiatric disease affecting evaluations
  • Multiple vessel occlusion (e.g., bilateral anterior circulation or both anterior and posterior circulation)
  • Brain tumors with mass effect (except meningiomas)
  • Intracranial aneurysm or arteriovenous malformation
  • Terminal illness with life expectancy less than 6 months
  • Unlikely to be available for 90-day follow-up

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 8 locations

1

Yijishan Hospital of Wannan Medical College

Wuhu, Anhui, China, 241000

Actively Recruiting

2

Xinqiao Hospital of Army Medical University

Chongqing, Chongqing Municipality, China, 400037

Not Yet Recruiting

3

Wuyi Traditional Chinese Medicine Hospital

Jiangmen, Guangdong, China, 529000

Not Yet Recruiting

4

The First Affiliated Hospital of Hainan Medical University

Haikou, Hainan, China, 570000

Actively Recruiting

5

Huai'an First People's Hospital

Huai'an, Jiangsu, China, 223001

Actively Recruiting

6

The 904th Hospital of CPLA

Wuxi, Jiangsu, China, 214000

Not Yet Recruiting

7

Jingdezhen First People's Hospital

Jingdezhen, Jiangxi, China, 333000

Actively Recruiting

8

Dalian Central Hospital

Dalian, Liaoning, China, 116000

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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