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Cerebral Venous Sinus ThrombosisCCCNCT03919305

Cerebral Venous Thrombosis Cohort Study in China Mainland

An observational study of Cerebral Venous Sinus Thrombosis and Deep Cerebral Vein Thrombosis, run by Capital Medical University at 1 site in China.

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Trial summary

This study was aimed to reveal the clinical features,natural history of the diseases and current therapeutic situations of cerebral venous thrombosis (CVT) in China mainland. Blood samples and cerebrospinal fluid samples will be collected after recruitment to reveal the pathological mechanisms of CVT and identify the… Read more about this study

Who is it for?
Any age
How many people
3,000 participants
Where
1 siteChina
Study dates
1 Jan 2019to 31 Dec 2026
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients with cerebral venous sinus thrombosis, deep cerebral vein thrombosis and cortical vein thrombosis.

Who may be able to join

  • Cerebral venous sinus thrombosis, deep cerebral vein thrombosis and cortical vein thrombosis diagnosed by digital subtraction angiography (DSA), magnetic resonance venography (MRV), computed tomography venography (CTV) or high-resolution magnetic resonance imaging (HR-MRI).

Who cannot join

  • None of the patient, trustee or immediate family members signed the informed consent.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Min Li, MD, PhD contact

+86-18701519698

812879698@qq.com

China1 site, 1 recruiting
  • Xuanwu Hospital, Capital Medical University

    Beijing

    Min Li, MD, PhD

    Recruiting

Other trials in China

About this study

This study was aimed to reveal the clinical features,natural history of the diseases and current therapeutic situations of cerebral venous thrombosis (CVT) in China mainland. Blood samples and cerebrospinal fluid samples will be collected after recruitment to reveal the pathological mechanisms of CVT and identify the biomarkers for CVT.

Read the detailed description

cerebral venous thrombosis (CVT) is caused by a clot in the cerebral vein, which resulted in an obstruction of the blood outflow. CVT mainly includes cerebral venous sinus thrombosis, deep cerebral vein thrombosis and cortical vein thrombosis. However, the epidemiological features of CVT in China mainland remained obscure. This study was aimed to establish a multicenter cohort recruiting patients with CVT across 31 provinces and municipalities in China mainland. Clinical features,natural history of the diseases and current therapeutic situations will be analyzed to reveal the epidemiological features of CVT. Blood samples and cerebrospinal fluid samples will be collected after recruitment to reveal the pathological mechanisms of CVT and identify the biomarkers for CVT. Patients will be followed-up at 1, 3, 6, 12 months from baseline to evaluate the clinical prognosis and therapeutic outcomes.

Keywords
Cerebral venous sinus thrombosis, Deep cerebral vein thrombosis, Cortical vein thrombosis, Cohort study, Real world evidence, Observational study, China mainland, Cerebral venous system thrombosis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Death rate

    A combination of death form of all causes

    Measured: 1 year from baseline

  2. Functional independence

    Defined as modified Rankin score (0-5) equal to or lower than 2

    Measured: 1 year from baseline

  3. Recurrence of cerebral venous sinus thrombosis, deep cerebral venous thrombosis and cortical vein thrombosis

    Diagnosed by DSA, MRV, CTV or HR-MRI

    Measured: 1 year from baseline

  4. Incidence of hemorrhagic complication

    Extracranial hemorrhage (fall in hemoglobin of 2 gram/dl or more within 48 hours) or intracranial hemorrhage

    Measured: 1 year from baseline

  5. Incidence of sinus wall rupture

    Measured: 1 year from baseline

  6. Incidence of acute ischemic stroke

    Measured: 1 year from baseline

  7. Incidence of acute myocardial infarction

    Measured: 1 year from baseline

  8. Incidence of pulmonary embolism

    Measured: 1 year from baseline

  9. Incidence of deep venous thrombosis

    Measured: 1 year from baseline

Secondary outcomes (2)
  1. Incidence of epilepsy

    Measured: 1 year from baseline

  2. Incidence of allergic reaction

    Measured: 1 year from baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Apr 2019
  2. Study start1 Jan 2019
  3. Primary completion31 Dec 2025
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
3,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03919305
Sponsor's protocol ID
CVT-China
Acronym
CCC
Status last verified
May 2026
First submitted
3 Apr 2019
Last updated
2 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

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