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A monocentric prospective randomized controlled trial on the effect of crystalloids and colloids on the cardiac stroke volume during neurosurgical spine surgery

A monocentric prospective randomized controlled trial on the effect of crystalloids and colloids on the cardiac stroke volume during neurosurgical spine surgery - Cybolix

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00022917
Enrollment
40
Registered
2020-09-04
Start date
2020-10-01
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

M43.9

Interventions

Group 1: fluid bolus of 250ml cristalloid/colloid over a 20 min period Group 2: fluid bolus of 250ml cristalloid/colloid over a 5 min period

Sponsors

Justus-Liebig-Universität GießenKlinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: informed consent male and female patients undergoing neurosurgical spine surgery in prone position (XLIF, TLIF, spondylodesis) Age > 18y ASA I - III general anaesthesia invasive blood pressure monitoring

Exclusion criteria

Exclusion criteria: age stage IIb) chronic kidney disease (> stage II according to KDIGO) pregnancy lack of consent participation in another (interventional) study

Design outcomes

Primary

MeasureTime frame
the change in cardiac stroke volume before and after intervention measured by non-calibrated hemodynamic monitoring

Secondary

MeasureTime frame
change in cardiac stroke volume > 10%, requirements for catecholamines (norepinephrine, epinephrine before and after the intervention µg/kg/min), change in mean arterial pressure (MAP), perioperative fluid balance, duration and AUC of hypotension (MAP < 65 mmHg)

Countries

Germany

Contacts

Public ContactMichael Sander

Justus-Liebig-Universität GießenKlinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie

martina.galfe@chiru.med.uni-giessen.de004964198544401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 12, 2026