Siemens Aktiengesellschaft

Markus Schmidt

Gudrun Zahlmann

Horst Schreiner

Siegfried Schneider

Rainer Alfred Kuth

Sebastian Schmidt

Klaus Abraham-Fuchs

Eva Rumpel

Björn Heismann

Patrick Gross

Martin Ringholz

Hanns Eder

Reto Merges

Kera Westphal

Norbert Rahn

Stefan Assmann

Martin Requardt

Ali-Nejat Bengi

Stefan Assman

A method is proposed for determining clinical study compliance. The method includes obtaining criteria for the clinical study and accessing stored clinical data relating to the clinical study. Thereafter, the criteria and clinical data are correlated to determine a measure of compliance with the criteria of the clinical study.

Method and system for measuring quality of performance and/or compliance with protocol of a clinical study

A method for determining electrical conduction path information in a chamber wall of a ventricle of a patient is provided. A three-dimensional magnetic resonance image data set is recorded showing the ventricles using a recording technology which allows an assignment of an electrical conductivity to a voxel based on the magnetic resonance image dataset. The chamber wall is segmented in the magnetic resonance image dataset. Conductivity determined from the image data is assigned to sub-regions of the chamber wall corresponding to individual voxels of the magnetic resonance image dataset. A model of the chamber wall is created as a function of the conductivities and segmentation. A conduction path information item is determined describing an electrical conduction path running from a start point to a destination point through the chamber wall in the model.

Method for determining electrical conduction path information in a chamber wall of a ventricle

A medical examination apparatus including a control unit, an image-generating modality and a controllable injection apparatus for a contrast agent is provided. The control unit is connected to an alarm signal emitter and the control unit switches the modality and the injection apparatus to a safe mode as a function of an alarm signal.

Medical examination apparatus having an alarm signal emitter

A control unit for an equipment arrangement is provided. The control unit includes an imaging modality, a measurement device for measuring a control variable and a controllable injection device for a regulatory substance influencing the control variable, wherein the injection rate of the injection device may be varied during a data acquisition such that a proposed value for the control variable is reached.

Control unit and medical examination apparatus

A patient support apparatus is provided. The patient support apparatus has a patient table, a movable support plate for supporting a patient, a guide unit, which is designed to guide the support plate along at least one movement direction of the support plate, and a fastening unit for fastening an auxiliary unit to the support plate. The fastening unit has at least one setting unit for setting the position of the auxiliary unit in relation to the support plate in a flexible manner.

Patient support apparatus and medical imaging apparatus having the patient support apparatus

A patient support apparatus, in particular for a medical imaging apparatus, has a table for supporting a patient, and a support unit, wherein the table is arranged at the support unit such that the table may be displaced along a longitudinal extension of the support unit. Further, the patient support apparatus has a protective wall element which closes off a region for receiving fluids on the table and/or on the support unit in a fluid-tight manner.

Patient support apparatus and medical imaging apparatus comprising the patient support apparatus

In a method for admitting an information provider to transmit information, a transmission device receives test data transmitted by an information provider, and the transmission device evaluates the quality of the test data. The test data represents information offered by the information provider. Depending on the quality of the test data, the transmission device admits the information provider to a system for transmitting information between information providers and information seekers. The transmission device then matches one or more information seekers with the information provider.

Method for admitting an information provider to a data transmission process, and transmission device

In a method for determining a parameter in an automatic study and data management system, data is gathered in a knowledge database, and a parameter is determined based the data gathered in the knowledge database. The data is correlated to at least one of a configuration and implementation of a previous clinical study. The parameter is usable for configuring a future clinical study.

Methods for determining parameters and planning clinical studies in automatic study and data management systems

A method is provided for configuring medical devices such as medical devices used in a clinical trial. Based on the needs of the clinical trial, a definition of a configuration of the medical devices to be used in the clinical trial is generated and the configuration data is transformed into a profile. The profile is distributed to sites at which the clinical trial will be conducted and the profile is applied to the medical devices at the sites to configure the medical devices. The medical devices are thereby capable of producing data that is comparable as between the sites used in the clinical trial.

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Nuremberg, Germany

Markus Schmidt