none
Conditions
Interventions
None listed
Sponsors
none
Eligibility
Inclusion criteria
Inclusion criteria: Healthy human volunteers older than 18 years old who conform to following criteria • Should not have any disease now including flu • Should not have any disease known before • Should not be under any medication • Should not drink coffee or eat meal in two hours before the procedure
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: • Volunteer who does not meet any of the criteria above • <18 years old • Pregnants • Maastad Ziekenhuis employers/colleagues • Refusal to participate in the study or demand to end study for any reason
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that the results from this project will provide new insights into the use and interpretation of different kind of LSCI devices in clinical practice and researches. •The primary objectives oTo test the comparebility of two different model LSCI devices in terms of baseline, supra- and infra-physiologic blood flows. oTo validate the non-validated LSCI device (Perimed (Järfälla, Sweden)) with a gold standart method (Cytocam-IDF). • | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objectives o To assess the response of the LSCI devices during PORH o To understand differences between the different kind of LSCI devices in terms of physiologic responses o To assess and define normal blood flow values of the normal population. | — |
Contacts
Public Contactannemieke dijkstra
Maasstad Ziekenhuis
Outcome results
None listed