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Multicenter Registry Study Of Cerebral Venous Thrombosis In China (RETAIN-CH)

A Registry Study of Cerebral Venous Sinus Thrombosis in China

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05448248
Enrollment
3276
Registered
2022-07-07
Start date
2022-08-20
Completion date
2023-12-20
Last updated
2024-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Vein Thrombosis, Cerebral Venous Sinus Thrombosis

Keywords

Cerebral Venous Sinus Thrombosis

Brief summary

This study will investigate the epidemiology, risk factors, diagnostics, treatment, and the long-term prognosis of cerebral venous thrombosis in China.

Detailed description

The epidemiology, risk factors, diagnosis and treatment of Cerebral Venous Thrombosis (CVT) in China are still unclear. A retrospective hospital-based study will be conducted at fifty different hospitals across 31 provinces in China. This study will use ICD-10 to search patients diagnosed with CVT between January 1, 2018 and June 15, 2022 across 31 provinces and municipalities of 104 hospitals in China. Risk factors, clinical and radiological findings, treatment and short-term outcomes will be recorded from the hospital record system. Finally, a prospective follow-up will be conducted for all of the patients enrolled above. By combining data collected from retrospective hospital records with the new follow-up, it will be possible to better understand the epidemiology, risk factors, diagnosis, treatment and the long-term prognosis of CVT in China.

Interventions

None listed

Sponsors

Brain Hospital of Hunan Provincial
CollaboratorUNKNOWN
The First Affiliated Hospital of Zhengzhou University
CollaboratorOTHER
The Affiliated Hospital of Xuzhou Medical University
CollaboratorOTHER
Guizhou Provincial People's Hospital
CollaboratorOTHER
Capital Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* 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).

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Favorable clinical outcome (modified Rankin score 0-1)Baseline to three years
All-cause mortalityBaseline to three yearsA combination of death form of all causes

Secondary

MeasureTime frameDescription
Headache after CVTBaseline to three yearsHeadache Impact Test - 6 score
Incidence of hemorrhagic complicationBaseline to three yearsExtracranial hemorrhage (fall in hemoglobin of 2 gram/dl or more within 48 hours) or intracranial hemorrhage
Recanalization rate of cerebral venous systemBaseline to three years
Recurrence of cerebral venous thrombosisBaseline to three yearsDiagnosed by DSA, MRV, CTV or HR-MRI
Incidence of acute ischemic strokeBaseline to three years
Incidence of pulmonary embolismBaseline to three years
Psychological distress after CVTBaseline to three yearsPopulation Health Questionnaire (PHQ)-9 score
Incidence of epilepsyBaseline to three years
Favorable clinical outcome (modified Rankin score 0-2)Baseline to three years

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026