Prehospital Emergency Care of Obstructive Respiratory Emergencies With the Use of Teleconsultation
NCT ID: NCT01644045
Last Updated: 2015-09-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
17 participants
INTERVENTIONAL
2012-08-31
2015-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Tracheal Intubation and Prehospital Emergency Setting
NCT03486171
Comparison of Airway Intubation Devices When Using a Biohazard Suit
NCT01924559
Out-of-Hospital Randomized Comparison of Video-assisted Endotracheal Intubation
NCT01635660
Infrared Transillumination of the Front of the Neck
NCT03930550
Topical Anesthesia / Bronchoscopy
NCT02237651
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Device: Teleconsultation
In cases of acute obstructive, respiratory emergencies if patients give informed consent the paramedics can use this system to contact a so called "tele-EMS physician" who has an audio-connection to the EMS team and receives vital parameters (e.g., ECG, pulse oximetry, non-invasive blood pressure) in real-time. The transmission of still pictures (taken with a smartphone), 12-lead-ECGs and video streaming from the inside of the ambulance can also be carried out, if indicated. The tele-EMS physician supports the EMS team in obtaining all relevant medical history, diagnosis and can delegate the application of medications. This can be carried out to bridge the time to the arrival of an EMS physician or in less severe cases without an EMS physician on-scene. The quality of prehospital care and the possible influences on the initial inhospital phase should be investigated and compared with regular EMS.
Teleconsultation
Teleconsultation for the EMS in acute respiratory emergencies
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Teleconsultation
Teleconsultation for the EMS in acute respiratory emergencies
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Verbal consent for teleconsultation obtained or patient is not able to consent due the severity of the emergency
Exclusion Criteria
* Refused consent for teleconsultation
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
RWTH Aachen University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Rolf Rossaint, Prof. Dr.
Role: STUDY_CHAIR
University Hospital Aachen, Germany, Department of Anesthesiology
Jörg C Brokmann, Dr.
Role: PRINCIPAL_INVESTIGATOR
University Hospital Aachen, Germany, Emergency Department
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Hospital Aachen
Aachen, , Germany
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PtJ-Az.: z0909im002b
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
005-1003-0034-4
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.