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Impact of a Standardized Alarming System on Treatment Times and Workflow in Stroke Patients With Interhospital Transfer for Thrombectomy

Impact of a Standardized Alarming System on Treatment Times and Workflow in Stroke Patients With Interhospital Transfer for Thrombectomy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05963685
Enrollment
280
Registered
2023-07-27
Start date
2022-09-16
Completion date
2024-03-15
Last updated
2023-07-27

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

Conditions

Acute Ischemic Stroke

Keywords

mechanical thrombectomy, telestroke, drip and ship, interhospital transfer, communication

Brief summary

The aim of this study is to evaluate the impact of a standardized alarming system on treatment times and workflow in stroke patients with interhospital transfer for mechanical thrombectomy (MT). The main questions it aims to answer are: * Is the implementation of a standardized alarming system associated with shorter transfer and treatment times? * Is the implementation of a standardized alarming system associated with a better adherence on existing standard operating procedures for interhospital transfer? We will analyze data from our existing thrombectomy registry comparing time periods before and after introduction of the MT alarming system.

Interventions

OTHERstandardized MT alarming system

Standardized alarming system via telephone loop in the primary thrombectomy centre triggered immediately after decision to mechanical thrombectomy in stroke patients admitted in primary stroke centers

Sponsors

Munich Municipal Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age \>= 18 years * diagnosis of acute ischemic stroke * indication for mechanical thrombectomy * admission to one of 7 participating primary stroke centers within in the catchment area of the referral center

Exclusion criteria

* unclear indication for mechanical thrombectomy (patients admitted for perfusion imaging before decision for or against a MT)

Design outcomes

Primary

MeasureTime frameDescription
decision-to-groin time24 hourstime from decision for MT (while patient still in the primary stroke center) to groin puncture (start of mechanical thrombectomy procedure in the primary thrombectomy center)

Secondary

MeasureTime frameDescription
decision-to-departure time24 hourstime from decision for MT to departure of the patient from primary stroke center (to the primary thrombectomy center)
decision-to-arrival time24 hourstime from decision for MT to arrival of the patient at the primary thrombectomy center
arrival-to-groin time24 hourstime from arrival of the patient at the primary thrombectomy center to groin puncture (start of mechanical thrombectomy procedure)
rate of refusal of transfer requests due to lack of capacity24 hoursrate of patients that had to be transferred to a secondary thrombectomy center instead of the primary thrombectomy centre due to lack of capacity in the referral clinic
Adverse events within 7 days7 daysAdverse events within the first 7 days after transfer to referral center
Periprocedural complications24 hoursrate of periprocedural complications during MT
Successful outcome of MT (mTICI > 2b)24 hoursrate of successfully performed MT (mTICI \> 2b) of all patients with attempted MT
groin-to-recanalization time24 hoursTime from groin puncture to successful recanalization
decision-to-transfer request time24 hoursTime from decision for MT to request of emergency medical service for interhospital transfer

Countries

Germany

Contacts

Primary ContactHanni Wiestler, MD
hanni.wiestler@muenchen-klinik.de+49 89 6210 5895
Backup ContactNikolai Hubert
+49 89 6210 3325

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026