No registrations found.
ID
Source
Brief title
Health condition
Multiple Sclerosis
Sponsors and support
Intervention
Outcome measures
Primary outcome
Investigating whether the AeonoseTM is able to distinguish breath of patients with confirmed diagnosis of MS and control subjects without any suspicion of MS.
Secondary outcome
Determining whether AeonoseTM patterns differ between patients with MS without medication and control subjects.
Determining whether AeonoseTM patterns differ for various types of MS.
Background summary
The primary aim of this study is to investigate whether an eNose can detect VOC patterns that
distinguish between patients with confirmed diagnosis of MS and matched subjects withou any suspicion of MS.
Study design: prospective, non-invasive case control study.
Study population: 100 patients diagnosed with MS, 100 control subjects.
Intervention: breathing through an eNose for 5 minutes.
There are no risks involved for the participants.
Study objective
We expect that MS could be detected by an electronic nose by analysing exhaled volatile compound patterns.
Study design
One measurement
Intervention
Participants will breathe through the AeonoseTM for 5 minutes.
Inclusion criteria
Inclusion criteria for patients with MS:
- Diagnosis MS had been confirmed by a neurologist.
- Age ≥ 18 years.
Inclusion criteria control subjects:
- Not suspicious of having MS.
- Age ≥ 18 years.
Exclusion criteria
Subjects who are physically or cognitively unable to use an eNose.
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL8146 |
| Other | METC Twente : METC K18-42 |