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Clinical Trials/NCT01811901
NCT01811901
Unknown
Not Applicable

Reduction of In-hospital Delays in Stroke Thrombolysis: SITS-WATCH

SITS International1 site in 1 country3,000 target enrollmentJanuary 2013
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
SITS International
Enrollment
3000
Locations
1
Primary Endpoint
Absolute DNT reduction of at least 20 minutes or at least 20% change in SITS-WATCH centers that completed the whole study period
Last Updated
13 years ago

Overview

Brief Summary

In patients with acute ischemic stroke: the sooner the thrombolysis treatment is administered after symptom onset - the better the outcome. This delay can be dissected into onset-to-door time and door-to-needle time (DNT). SITS-WATCH aims to reduce median DNT in participating centres.

Detailed Description

In patients with acute ischemic stroke: the sooner the thrombolysis treatment is administered after symptom onset - the better the outcome. This delay can be dissected into onset-to-door time and door-to-needle time (DNT). Of the two, DNT can be directly influenced within the hospital by stream-lining of acute stroke care. The aim of our study is to reduce in-hospital delays (DNT) in self-selecting centers recruiting patients into the the Safe Implementation of Treatments in Stroke-International Stroke Thrombolysis Register (SITS-ISTR) , comprising currently more than 80 000 patients from 1338 centers. Current median of DNT in all SITS centers is 65 minutes (compared with 20 minutes in Helsinki Univer-sity Central Hospital). An itemized detailed questionnaire, including all factors known to influence DNT, has been sent to all SITS centers to identify the reasons for long in-hospital delays. Based on the replies, we have prepared a list of interventions that can be considered by individual SITS centers in order to reduce DNT with interventions that are in line with national legislation.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
June 2015
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
SITS International
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All consecutive patients with acute ischemic stroke registered in SITS registry.

Exclusion Criteria

  • Centers not inputing patient data into SITS registry. Patients with missing DNT data.

Outcomes

Primary Outcomes

Absolute DNT reduction of at least 20 minutes or at least 20% change in SITS-WATCH centers that completed the whole study period

Time Frame: January 2013-December 2014

DNT will be evaluated at regular intervals (twice a year).

Secondary Outcomes

  • Significantly larger reduction of DNT in SITS-WATCH centers compared with non-SITS-WATCH centers in SITS.(2014-2015)

Study Sites (1)

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