Intraoperative, continous non invasive haemoglobin measurement in infants and children

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00004188

Enrollment

Registered

2012-07-10

Start date

2011-12-28

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

D64

Interventions

Group 1: Children under the age of 6 years undergoing regular bigger surgeries. The hemoglobin concentration is going to be controlled as well as Masimo Pronto 7 and taken blood samples.

Eligibility

Sex/Gender

All

Age

0 Months to 6 Years

Inclusion criteria

Inclusion criteria: patients under the age of 6 years undergoing relevant surgeries

Exclusion criteria

Exclusion criteria: patients with band aid allergy; patients who are already included into another clinical trial; parent´s refusal to participate the study; patients with diseases of the hemoglobin chain

Design outcomes

Primary

Measure	Time frame
There is a correlation between the total Hemoglobin measured by Masimo Pronto 7 and the tHb in the blood samples.	—

Secondary

Measure	Time frame
hte aim is to evaluate if the medical product can be used in clinical practise after 30 patients there should be estimate a bland atman analysis	—

Countries

Austria

Contacts

Public ContactLydia Triffterer

Medizinische Universität Wien

lydia.triffterer@meduniwien.ac.at+43 1 40 400 5262

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026