Status:

COMPLETED

Temporal Trends of Thrombolysis Treatment in Chinese Acute Ischemic Stroke (AIS) Patients From 2007-2017: Analysis of China National Stroke Registry (CNSR) I, II, and III; CTP-Draft Review Performed;

Lead Sponsor:

Boehringer Ingelheim

Conditions:

Stroke

Eligibility:

All Genders

18-80 years

Brief Summary

The present study is to be conducted based on the AIS patient data collected from CNSR I, II, and III. The primary objectives are: * To investigate the temporal changes in the proportion of intraven...

Eligibility Criteria

Inclusion

  • Patient group A: All AIS patients
  • Aged 18 80 years
  • Diagnosed with AIS on admission
  • Patient groups B and B': IVT eligible patients
  • Met the in- and exclusion criteria of "all AIS patients"
  • Arrived at hospital within 2 h (patient group B) or 3.5 h (patient group B') of symptom onset
  • Patient groups C and C': IV rtPA treated patients
  • Met the in- and exclusion criteria of "IVT eligible patients"
  • Treated with IV rtPA within 3 h (patient group C) or 4.5 h (patient group C') of symptom onset

Exclusion

  • Patient group A: All AIS patients
  • Missing baseline data including age and gender
  • Diagnosed with intracranial hemorrhage (ICH), Transient Ischemic Attack (TIA), subarachnoid hemorrhage (SAH), or unspecific stroke
  • Arrived at hospital after 7 days of symptom onset
  • Patient groups B and B': IVT eligible patients
  • Missing key data including:
  • i. symptom onset time (or last known well time) ii. hospital arrival time iii. whether received IVT treatment or not iv. the time of IVT treatment
  • Documented IVT absolute contraindications, according to the case report form (CRF) for each wave of CNSR
  • Patient groups C and C': IV rtPA treated patients
  • Not received IVT
  • Received IVT other than rtPA
  • Treated with IV rtPA after 3 h (patient group C) or 4.5 h (patient group C') of symptom onset
  • Received additional treatments with intra arterial reperfusion or experimental therapies

Key Trial Info

Start Date :

September 21 2020

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

September 30 2020

Estimated Enrollment :

42188 Patients enrolled

Trial Details

Trial ID

NCT04290494

Start Date

September 21 2020

End Date

September 30 2020

Last Update

November 5 2021

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Beijing Tiantan Hospital

Beijing, China, 100070