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Quantification of Transition Metals

Quantification of Transition Metals in Patients at the Cologne University Hospital

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02222779
Enrollment
3000
Registered
2014-08-21
Start date
2014-09-30
Completion date
Unknown
Last updated
2014-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infections, Neurodegenerative Diseases

Brief summary

In this trial, concentrations of transition metals of interest are quantified in surplus cerebrospinal fluid (CSF) and blood serum samples. Quantification of the transition metals will be performed by inductively coupled plasma mass spectrometry (ICP-MS). The treating physicians as well as the patients will not be informed about the results of drug concentrations.

Detailed description

Samples used include: Remaining portions of samples collected for diagnostic or therapeutic reasons (paired CSF and blood serum samples). No lumbar puncture will be done specifically for this protocol. The objective of this study is to gain an overview about transition metals concentrations in blood serum and CSF in order to provide preliminary data on patients. The effect of neurodegenerative diseases on metals or the other way round will be assessed if possible.

Interventions

None listed

Sponsors

University of Cologne
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

• * The trial will include any patient (with various diseases, especially neurodegenerative diseases) who received a lumbar puncture.

Exclusion criteria

* • The lower age limit is 18 years. In concordance with the objective of the project there is no specific

Design outcomes

Primary

MeasureTime frame
Transition metal concentration5 years

Countries

Germany

Contacts

Primary ContactUwe Fuhr, Professor
uwe.fuhr@uk-koeln.de0049221478

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026