Condition: Surgery-Complications · Medical Complication · Sponsor: Rigshospitalet, Denmark
Aim: to assess the validity of CE/FDA approved vital sign monitor devices for clinical use in clinical setting. Patients: up to 1000 medical and/or surgical patients will be included Intervention: Studies with various wirless or novel vital sign monitor devices control: Golden standard measurements or clinical standard devices Outcome: Agreement assessed by bias and limits of agreement between Intervention and control device.
This description comes directly from the study's public registry record.
Eske K Aasvang, DMSci · +4526232076 · eske.kvanner.aasvang.01@regionh.dk
Christian S Meyhoff, PhD · +4524910542 · Christian.sylvest.meyhoff@regionh.dk
Always discuss trial participation with your own doctor first.
| Eske Kvanner Aasvang | Copenhagen, Denmark | Recruiting |
| Bispebjerg Hospital | Copenhagen, Denmark | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT06106516