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Med-on-@ix: Telemedical support for prehospital Emergency Medicals Services in a prospective controlled trial

T-EMS2-Trial: TEleMedical Support in Emergency Medical Services in a prospective controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN83270177
Enrollment
1000
Registered
2010-05-18
Start date
2010-05-01
Completion date
Unknown
Last updated
2017-10-16

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

Conditions

Acute stroke

Interventions

The study will be held in the EMS of Aachen. Within a period of five months totally, all inhabitants who have to make use of the EMS by calling the nationwide emergency phone number 112, will receive

Sponsors

University Hospital Aachen (Germany)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients who calls EMS in Aachen, Germany from May 1st to September 30th 2010 (as of 17/05/2011; March 1st to July 31st 2010 at time of registration)

Exclusion criteria

Exclusion criteria: Does not match inclusion criteria

Design outcomes

Primary

MeasureTime frame
1. Guideline coherence for stroke and acute coronary syndrome: measured with data of the medical records / EMS-documentation 2. Improved treatment time intervals for stroke and ST-Elevation myocardial infarction 2.1. on scene time (all patients) 2.2. call to hospital arrival time (all patients) 2.3. call to PCI time (STEMI) 2.4. call to computed tomography time (stroke) 2.5. call to thrombolysis time (stroke) All time intervals are measured with the computer system of the EMS dispatch centre and the computer systems of the hospitals. Both are synchronised. 3. improved patient safety and patient outcome 3.1. documentation of critical events, evaluated with medical records 3.2. length of hospital stay, evaluated with medical records 3.3. mortality, evaluated with medical records 4. Improved choice of appropriate hospital respiratory facility comparison of the diagnosis and the level of the receiving hospital, evaluated with medical records 5. Improved quality of pre-hospital diagnosis comparison between diagnosis in EMS and the diagnosis in hospital, evaluated with medical records 6. Improved quality of documentation in respect of medical and research purposes. comparison between data quality in standard EMS (paper based documentation) and EMS with TMA (electronic documentation with integrated plausibility check)

Secondary

MeasureTime frame
The usability and feasibility of the system as well as the percentage of safe transferability of monitoring data will be observed and used for further improvement of the system. These criteria are measured with predefined checklists, which have to been completed after each mission with TMA.

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 26, 2026