The largest database of trusted experimental protocols

Tomoscan sr7000

Manufactured by Philips
Sourced in Netherlands

The Tomoscan SR7000 is a medical imaging device manufactured by Philips. It is a computed tomography (CT) scanner that produces cross-sectional images of the body. The Tomoscan SR7000 uses X-ray technology to create detailed images of the internal structures of the body, which can be used for diagnostic and clinical purposes.

Automatically generated - may contain errors

7 protocols using tomoscan sr7000

1

Multimodal Neuroimaging for Surgical Planning

Check if the same lab product or an alternative is used in the 5 most similar protocols
For each patient included in the study a T1-weighted structural pre-operative MRI scan was acquired on a 3T scanner (Philips Achieva, Best, the Netherlands), with an isotropic voxel size of 1 mm. Cortical surface segmentation of each subject’s anatomy was performed using FreeSurfer (https://surfer.nmr.mgh.harvard.edu/). Additionally, a post-operative high-resolution 3D-CT scan was acquired to locate the electrodes (Philips Tomoscan SR7000), with voxel sizes of 0.49 mm × 0.49 mm × 1 mm for subjects S3–6, S10, S14 and S15; 0.49 mm × 0.49 mm × 0.7 mm for subjects S1–2, S7, S13, S16 and S17; 0.49 mm × 0.49 mm × 0.45 mm for subjects S8–9 and S11; and, lastly, 0.43 mm × 0.43 mm × 0.5 mm for subject S12. Resolutions differed due to availability of one of multiple CT scanners at the time of the clinical CT scan.
+ Open protocol
+ Expand
2

Localizing Epileptic Seizure Origin with ECoG

Check if the same lab product or an alternative is used in the 5 most similar protocols
In this study we included seven individuals with epilepsy (mean age 28; Table 1). The participants were implanted with subdural ECoG grids and strips (inter-electrode distance 1 cm center-to-center and 2.3 mm exposed surface; Ad-Tech, Racine, USA) to localize the origin epilepsy. They agreed to participate in this study and signed informed consent according to the Declaration of Helsinki (2013). The study was approved by the Medical Ethical Committee of the University Medical Center Utrecht.
The ECoG grids and strips fully or partially covered the hand region of the sensorimotor cortex. The exact location and number of electrodes differed per participant (Figure 1) and depended on the clinical plan to determine the epileptic seizure onset location. Electrodes were localized with a procedure described in Hermes et al. (2010) (link) and Branco et al. (2018) (link), where a post-implantation Computerized Tomography (CT) scan (Philips Tomoscan SR7000, Best, the Netherlands) is co-registered with a pre-implantation T1-weighted anatomical magnetic resonance imaging (MRI) scan (Philips 3T Ingenia or 7T Achieva, Best, the Netherlands; 1 mm isotropic), and displayed on a Freesurfer pial surface (recon-all, http://surfer.nmr.mgh.harvard.edu/).
+ Open protocol
+ Expand
3

Mapping Visual Cortex with ECoG

Check if the same lab product or an alternative is used in the 5 most similar protocols
Four subjects (one female) underwent implantation of ECoG grids for the purpose of epilepsy monitoring. The study was approved by the medical ethical board of the Utrecht University Medical Center. All subjects gave their written informed consent to participate in the study in compliance with the Declaration of Helsinki 2013. All participants had normal or corrected-to-normal vision and the epileptogenic tissue did not extend to the hMT+ area under examination. Data were recorded with a 128 channels Micromed system (Treviso, Italy) at a sampling rate of 512 Hz and band-pass filtered between 0.15–134.4 Hz. Implanted grids had 1 cm inter-electrode spacing and electrodes had a diameter of 2.3 mm. For each subject, electrodes were localized on a post-surgery high-resolution computed tomography scan (Philips TomoscanSR7000) and projected on the cortical surface obtained by a pre-surgical anatomical MRI [Branco et al., 2016 ; Hermes et al., 2010 (link)].
+ Open protocol
+ Expand
4

Epilepsy Patients ECoG Grid Study

Check if the same lab product or an alternative is used in the 5 most similar protocols
We included 12 epilepsy patients (mean age 27, range 15-49; see Table 1) who were implanted with subdural
ECoG grids to localize the seizure focus. Two types of grids were used. Standard
ECoG grids had an inter-electrode distance center-to-center of 1 cm and 2.3 mm
exposed surface diameter, whereas high-density grids had either 32 or 64
channels, with 1.3 mm exposed surface diameter and an inter-electrode distance
of 3 mm center-to-center (all AdTech, Racine, USA). For the following analysis,
some electrodes were excluded because they showed flat or unstable signals, or
high power-line noise levels. From the remaining electrodes, only those located
over sensorimotor cortex (as determined by visual inspection, see Figure 1) were considered for further
analysis. For this, the electrodes were localized using co-registration between
a post-implantation Computerized Tomography (CT) scan (Philips Tomoscan SR7000,
Best, the Netherlands) and a pre-operative T1-weighted anatomical scan on a 3T
Magnetic Resonance system (Philips 3T Achieva, Best, the Netherlands), corrected
for brain shift (Hermes et al., 2009 (link);
Branco et al., 2017b ) and projected on
a cortex surface rendering (Figure 1). The
Medical Ethical Committee of the Utrecht University Medical Center approved the
study and all patients signed informed consent according to the Declaration of
Helsinki (2013).
+ Open protocol
+ Expand
5

Localizing Epileptic Foci with fMRI and ECoG

Check if the same lab product or an alternative is used in the 5 most similar protocols
Subjects (three males, one female) were epilepsy patients who underwent implantation of subdural electrode grids to determine the site of epileptic foci for the purpose of possible surgical removal of the epileptogenic tissue. Implanted grids extended to healthy tissue in the hMT+ area of the left (n=2) and right (n=2) hemisphere. Before the subdural electrode implantation, subjects underwent an fMRI scan and were presented with visual motion stimuli identical to the ones performed during ECoG measurements, except that the presentation timing was adjusted to match the timing of the hemodynamic (fMRI) responses. A high resolution (0.5×0.5×1mm) 3D computed tomography (CT, Philips TomoscanSR7000) scan was acquired after implantation to localize ECoG grid electrodes on each subjects brain. The study was approved by the medical ethical board of the Utrecht University Medical Center. All subjects gave their written informed consent to participate in the study in compliance with the Declaration of Helsinki 2013.
+ Open protocol
+ Expand
6

Localization of ECoG Electrodes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Data from 8 patients who underwent surgery for removal of their focus of epilepsy were used. Six subjects (S1-S6) were implanted with ECoG grids 5-7 days before resection (chronic grids) and two only underwent ECoG during surgery (acute grids). All patients were implanted with high-density (HD) ECoG grids (Table 1) and gave consent to participate in the study. For 5 subjects (S1-3 and S5-6), the electrode positions, as predicted with the new GridLoc method (detailed below), were compared with locations obtained with a standard localization method (Hermes et al. 2010 (link); Branco et al. 2017b (link)), where the clinical post-operative CT scan (Philips Tomoscan SR7000, Table 1) was co-registered with their structural MRI scan. For the other three subjects (S4, chronic grid; and S7 and S8, acute grids) the GridLoc electrode positions were compared with (visible) locations determined with intra-operative photographs (Hermes et al. 2010 (link)). The study was approved by the ethical committee of the University Medical Center Utrecht, in accordance with the Declaration of Helsinki (2013).
+ Open protocol
+ Expand
7

Identifying Significant Brain Regions in Motor Tasks

Check if the same lab product or an alternative is used in the 5 most similar protocols
Electrode selection was based on the individual response to task 1. Electrodes with a significant response to task 1 were selected per run with a paired t-test (p < 0.05, Bonferroni corrected) between rest and active HFB mean values (rest period -2 to -1 s and active period -1 to 0 s, both relative to the peak of force; see also Figure 3). When a subject performed more than one run, the union of the significant channels of individual runs was used. Significant electrodes were grouped into four regions-of-interest (ROIs), depending on their cortical region (Figure 2, Table 3): all electrodes (in- and out-side the SMC), electrodes over M1, electrodes over central sulcus and electrodes over S1. For this purpose, the electrodes were localized by co-registering a pre-operative T1-weighted anatomical magnetic resonance imaging (MRI) scan (Philips 3T Achieva, Best, the Netherlands) with a post-implantation computerized tomography (CT) scan (Philips Tomoscan SR7000, Best, the Netherlands). The electrode locations were corrected for brain shift and projected on a cortex surface rendering (Branco et al., 2018 (link); Hermes et al., 2010 (link)). In total, four averaged signals were used in the following analysis, each representing the mean HFB signal across one of the four ROIs.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!