Skip to content

Intraoperative Volume Management and QT Interval

Intraoperative Repolarisation - Etiology and Relevance for the Decision Making by Anesthesiologists in the Management of Volume Substitution and Transfusion

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02441751
Enrollment
200
Registered
2015-05-12
Start date
2015-05-31
Completion date
2023-12-31
Last updated
2022-03-31

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

Conditions

Blood Loss, Surgical

Keywords

Electrocardiography, Hemorrhage, Monitoring, Intraoperative

Brief summary

QT interval changes is measured during all phases of the operation. The protocol is focusing at intraoperative bleeding events and is also observing QT interval changes during anesthetic and operative procedures.

Detailed description

Prolongation of the QT interval is associated with functional torsade de points, re-entry, and sudden death (see reference). Variations of QT-interval caused by changes in the volume status of the patient during an operation remained unclear. QT interval changes will be monitored during the surgery with the focus of the influence of sudden blood loss, volume substitution by crystalloids, blood and blood products. The effect of surgical procedures on the QT-interval (e.g. clamping of kidney artery) will be observed as well as the association of intra-operative QT-interval alterations with postoperative complications.

Interventions

PROCEDUREintra-operative blood loss

surgery in the urology and orthopedics

Sponsors

Technische Universität Dresden
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* American Society of Anesthesiologists physical status classification 2 - 3 * patients after consent

Exclusion criteria

* Children, * pregnant women, * patients not able to consent

Design outcomes

Primary

MeasureTime frame
change in QT-timeduring operation

Secondary

MeasureTime frameDescription
postoperative incidents/disturbance rhythm of the heart2 daysassociation to intraoperative repolarisation-disturbance / QT-prolongation
survival1 yearassociation to intraoperative repolarisation-disturbance / QT-prolongation

Countries

Germany

Contacts

Primary ContactTorsten Richter, M.D.
torsten.richter@uniklinikum-dresden.de004935145818034
Backup ContactJuliane Flaxa, M.D.
juliane.flaxa@uniklinikum-dresden.de0049351458

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026