Instant- Diagnostic of Bleeding for intraoperative Optimization of Therapy

Instant- Diagnostic of Bleeding for intraoperative Optimization of Therapy - SUBITO

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00005082

Enrollment

500

Registered

2013-10-09

Start date

2013-10-14

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

Intra- and postoperative coagulation abnormalities, focus: kardiac-sugery D65 D68 D69

Interventions

Group 1: Cases undergoing intraoperative routine diagnostic with point-of care tools (ROTEM) plus conventional coagulation lab measurements Group 2: Historic control cases in which the diagnostic tool

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: written informed consent

Exclusion criteria

Exclusion criteria: missing informed consent

Design outcomes

Primary

Measure	Time frame
Incidence of bleeding	—

Secondary

Measure	Time frame
Duration of hospitalization, ICU stay, rates of infections, duration of ventilation, mortality	—

Countries

Germany

Contacts

Public ContactStephan Sixt

Klinik für AnästhesiologieUniversitätsklinik Düsseldorf

stephanurs.sixt@med.uni-duesseldorf.de0211 81 18101

Outcome results

None listed

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