The largest database of trusted experimental protocols

Gyroscan nt 1

Manufactured by Philips
Sourced in Netherlands

The Gyroscan NT 1.5 is a magnetic resonance imaging (MRI) system developed by Philips. It operates at a field strength of 1.5 Tesla and is designed for clinical imaging applications.

Automatically generated - may contain errors

Lab products found in correlation

2 protocols using gyroscan nt 1

1

Gadolinium-Enhanced MRI for Neurological Assessment

Check if the same lab product or an alternative is used in the 5 most similar protocols
All subjects underwent gadolinium (Gd)-enhanced MRI (brain and spinal cord). MRI was performed in all the patients with a 1.5-T magnet (Philips Gyroscan NT 1.5), with sequences Flair, T2- and T1-weighted after Gd. The presence of at least one Gd-enhancing lesion or of at least one new/enlarging T2-hyperintense lesion was considered indicative of disease activity at MRI.
+ Open protocol
+ Expand
2

Longitudinal MRI Assessment of MS

Check if the same lab product or an alternative is used in the 5 most similar protocols
All MRI scans were performed on a 1.5 Tesla magnet (Philips Gyroscan NT 15, Netherlands) at baseline, month 12 and month 24. The MRI protocol included proton density-and T2-weighted spin echo images (TR 2000 ms, TE 20/90 ms, matrix size 256×256, field of view 24 cm×24 cm, slice thickness 3 mm, gap 0 mm, 48 axial slices) and T1-weighted images (TR 600 ms, TE 15 ms, matrix size 256×256, field of view 24 cm x 24 cm, slice thickness 3 mm, gap 0, 48 axial slices) obtained before and five minutes after an intravenous injection of 0,1 mmol/kg of gadoliniumdiethylenetriamine penta-acetic acid (Gd).
Volumes of hyperintense lesions on T2-weighted images (T2-LL), hypointense lesions on T1weighted post-contrast images (T1-LL) and hyperintense lesions on T1-weighted post-contrast images (T1-Gd-LL) were quantified using a semi-automated method (Jim 4.0, Xinapse System, Leicester, UK). The number of patients with Gd-enhancing lesions at baseline and at month 24 was calculated for each group. The cumulative number of combined unique active (CUA) lesions, defined as new Gd enhancing lesions or new T2-weighted lesions (non-enhancing on post-contrast T1-weighted acquisitions, in order to avoid double-counting), was also quantified at month 24.
+ 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!