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Magnetom trio 3t mr scanner

Manufactured by Siemens
Sourced in Germany

The Magnetom Trio 3T MR scanner is a magnetic resonance imaging (MRI) device manufactured by Siemens. It operates at a magnetic field strength of 3 Tesla, providing high-quality imaging capabilities for a variety of clinical applications.

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11 protocols using magnetom trio 3t mr scanner

1

Simultaneous MRI-PET Imaging with High Spatial Resolution

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All measurements were performed on a 3T MR-BrainPET developed by Siemens (Siemens Healthcare, Erlangen, Germany) as a prototype.16 (link), 17 (link) The BrainPET is operated as an insert within a slightly modified Siemens 3T MAGNETOM Trio MR scanner. The BrainPET insert is MR compatible and has high-resolution PET detectors with an axial field of view of 19.2 cm and an inner diameter of 32 cm. Each detector module has a 12 × 12 matrix of 2.5 × 2.5 × 20 mm3 individual lutetium oxyorthosilicate crystals coupled to a 3 × 3 array of avalanche photo diodes. Six detector modules are aligned within a copper-shielded cassette, and 32 such cassettes constitute the cylindrical PET detector that has an outer diameter of 60 cm enabling it to fit inside the bore of the MR scanner. Two dedicated MR head coils, consisting of an outer birdcage transmit coil and an inner 8-channel receive coil, were optimized with regard to minimal PET attenuation and are placed in the PET detector. PET images acquired with the MR-BrainPET have an excellent spatial resolution of 3 mm.18 (link) Simultaneous acquisition of MRI and PET data sets can be carried out without any notable interference between the two modalities.18 (link)
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2

Multimodal MRI Protocol for Perfusion Imaging

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MRI was performed using a Siemens 3T Magnetom Trio MR scanner. Anatomical MRI included a T1-weighted MPRAGE sequence (T1), T2-weighted FLAIR sequence (FLAIR) and contrast-enhanced T1-weighted MPRAGE sequence (T1c) conducted 3 min after injection of the contrast agent gadoteric acid (DOTAREM; Guerbet) with a dose of 0.1–0.2 mmol/kg body weight. A dynamic susceptibility-weighted contrast-enhanced T2* sequence (DSC) measuring the first pass of a contrast agent bolus (single shot echo planar imaging sequence (EPI) was used for PWI: dynamic interscan interval = 1500 ms; echo time (TE) =32 ms; flip angle = 90°, image matrix = 128 × 128, field of view FOV = 230 mm × 230 mm, slice thickness 5 mm). The contrast agent was injected with a power injector Injektron 82 MRT (Medtron AG) via an 18–20-gauge intravenous catheter at a dose of 0.1 mmol/kg body weight (flow rate, 5 ml/s). Parametric rCBV maps were created from DSC MRI data using the software Stroketool version 2.7 [28 (link)].
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3

T1-weighted MRI Acquisition Protocol

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The subjects were scanned, and T1-weighted (T1) images were acquired using a Siemens 3T MAGNETOM Trio MR scanner (Siemens, Erlangen, Germany). For the T1 images, a three-dimensional (3D) magnetization-prepared rapid acquisition gradient-echo (MPRAGE) sequence and the following imaging parameters were used: repetition time, 1670 ms; echo time (TE), 1.89 ms; voxel size, 1.0 × 0.98 × 0.98 mm3; field of view, 250 mm; flip angle, 9°; and 208 slices. To ensure quality control, the acquired MRI images were visually inspected for any artifacts or malformation of brain structures.
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4

3T MRI Protocol for Structural Brain Imaging

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An anatomical 3D T1-weighted MP-RAGE sequence with matrix size = 256 × 256 × 192; voxel size = 1 × 1 × 1 mm; TR/TE/TI = 1550/3.04/800 ms; flip angle = 9° was acquired for all patients using a Siemens Magnetom Trio 3T MR scanner or a Siemens 3T Verio MR scanner. In addition, a 3D T2-weighted isotropic sagittal sequence with matrix size 256 × 256 × 176; voxel size = 1 × 1 × 1 mm; TR/TE = 3200/409 ms; flip angle = 120° was also acquired for all subjects. All single-subject MRI sequences were corrected for gradient nonlinearities according to Jovicich et al. 2006 (link), in order to correct for spatial distortions and achieve optimal PET-MR co-registration. All the acquired MR images were examined for structural abnormalities, as a criterion for subject inclusion.
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5

3T fMRI Scanning Protocol for Cognitive Studies

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MRI scanning was conducted on a Siemens MAGNETOM Trio 3 T MR Scanner at the Henry H. Wheeler, Jr. Brain Imaging Center at the University of California, Berkeley. Anatomical images consisted of 160 slices acquired using a T1-weighted MP-RAGE protocol (TR = 2300 ms, TE = 2.98 ms, FOV = 256 mm, matrix size = 256 × 256, voxel size = 1 mm3). Functional images consisted of 24 slices acquired with a gradient echoplanar imaging protocol (TR = 1370 ms, TE = 27 ms, FOV = 225 mm, matrix size = 96 × 96, voxel size = 2.3 × 2.3 × 3.5 mm). A projector (Avotec SV-6011, http://www.avotecinc.com, Stuart, Florida) was used to display the image on a translucent screen placed within the scanner bore behind the head coil. A mirror was used to allow the subject to see the display. Subjects made their responses via an MRI-safe fiber optic response pad (Inline Model HH-1 × 4-L, http://www.crsltd.com, Rochester, Kent, UK).
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6

Multimodal MRI-based GBM Segmentation

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Magnetic resonance imaging was performed using a Magnetom Trio 3T MR scanner (Siemens Healthcare, Erlangen, Germany) in all patients with brain metastases. For the 354 patients with GBM at the Tiantan Hospital, Magnetom Trio 3T MR scanner was used in the 253 patients. In the remaining 101 patients, MRI was performed using Sigma 3T MR scanner (General Electric Company). For T2-weighted images, the specifications were as follows: repetition time, 4,500–6,000 ms; echo time, 84–122.5 ms; slice thickness, 3–5 mm; field of view, (180–240) mm × (219–256) mm; and matrix size, (160–512) × (208--512) pixels. For CE images, enhancement was achieved by injecting gadolinium-diethylenetriamine penta-acetic acid (0.1 mmol/kg, Beijing Beilu Pharmaceutical, Beijing, China), and the acquisition parameters were as follows: repetition time, 560--2520 ms; echo time, 2.3--19.7 ms; and slice thickness, 3--5 mm. The MR images of GBMs from the TCGA database were downloaded from the Cancer Imaging Archive.1Lesions were manually segmented on T2-weighted images (tumor and peritumoral edema area) and CE images (tumor area) by two neurosurgeons using MRIcro.2 Segmentation was evaluated by a neuroradiologist with more than 20 years of experience in brain tumor diagnosis.
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7

3D T1-Weighted MRI Protocol for PET-MR Co-registration

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An anatomical 3D T1-weighted MP-RAGE sequence with matrix size = 256 × 256 × 192; voxel size = 1 × 1 × 1 mm; TR/TE/TI = 1550/3.04/800 ms; flip angle = 9° was acquired for all patients using a Siemens Magnetom Trio 3T MR scanner or a Siemens 3T Verio MR scanner. All single-subject MRI sequences were corrected for gradient nonlinearities according to Jovicich et al. (2006 (link)), in order to correct for spatial distortions and achieve optimal PET-MR co-registration. All of the acquired MR images were examined for structural abnormalities, as a criterion for subject inclusion.
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8

Resting-State fMRI Acquisition Protocol

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Functional MRI data were acquired on a Magnetom Trio 3T MR Scanner (Siemens AG, Erlangen, Germany). During the resting-state fMRI session, the participants were instructed to relax with their eyes closed and keep their heads still during the scans. Functional images were subsequently acquired in the same slice orientation with a GRE-EPI (gradient recalled echo, echo-planar imaging) sequence (TR/TE = 2,000 ms/30 ms, FOV 24.0 × 24.0 cm2, FA 90°, matrix 64 × 64, slice thickness 4.0 mm, slice gap 0.4 mm, 30 slices, acquisition voxel size = 3.0 × 3.0 × 3.0 mm) for eight minutes and twenty seconds (250 measurements). 3D T1-weighted images were also acquired by using a 3DMPRAGE sequence, matrix 256 × 256, slice thickness 1.0 mm.
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9

Structural and Resting-State fMRI Acquisition

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MRI scanning was conducted on a Siemens MAGNETOM Trio 3T MR Scanner at the Henry H. Wheeler, Jr. Brain Imaging Center at the University of California, Berkeley. Anatomical images consisted of 160 slices acquired using a T1-weighted MP-RAGE protocol (TR = 2300 ms, TE = 2.98 ms, FOV = 256 mm, matrix size = 256 x 256, voxel size = 1 mm3). Resting state functional images were obtained while subjects were lying quietly with eyes open, and consisted of 35 slices acquired with a gradient echoplanar imaging protocol (TR = 1900 ms, TE = 24 ms, FOV = 225 mm, matrix size = 96 x 96, voxel size = 3.0 mm x 3.0 mm x 3.5 mm).
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10

Functional MRI and Structural Brain Imaging

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All MRI scans were acquired using a Siemens MAGNETOM Trio 3T MR scanner at the Imaging Center for Brain Research at Beijing Normal University. Foam padding and a plastic brace were used to minimize head movement. For the functional imaging, the whole-brain coverage of 33 axial slices was acquired using a T2-weighted echo-planar imaging sequence based on the blood oxygenation level-dependent (BOLD) contrast with the following parameters: 2000 ms repetition time (TR), 30 ms echo time (TE), 90° flip angle, 4.0-mm slice thickness, 0.6-mm gap, 64 × 64 data matrix, 200-mm field of view (FOV), and 3.1 × 3.1 × 4.0-mm voxel size. In addition, 3D structural brain scans were also acquired for each participant using a T1-weighted anatomical scan with the following parameters: 2530-ms TR, 3.39-ms TE, 7° flip angle, 256 × 256 data matrix, 256-mm FOV, 1.3 × 1.0 × 1.3-mm voxel size, and Bandwidth (BW) = 190 Hz/pixel.
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