NCT Number: NCT02978066
Postspinal Hypotension and Cardiac Performance in the Elderly
Patients, scheduled for elective arthroplasty were monitored with Lithium Dilution Cardiac Output monitor (LiDCOplus™) before and 45 minutes after spinal anesthesia. Hypotension was defined as systolic blood pressure ≤ 100 mmHg or ≥ 30% decrease from baseline. Associations between hypotension and the hemodynamic changes after preanaesthetic fluid loading and spinal anesthesia were analysed by logistic regression analyses.
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Notify MeKey information
Conditions
Age range
65 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- hip or knee arthroplasty
- spinal anaesthesia
- age 65 years or more
Exclusion criteria
- weight <40kg
- concomitant lithium medication
- written informed consent not obtained
- research team unavailable
Treatment and study plan
Primary outcomes
-
Stroke volume in ml
Time frame: 0-45 minutes after spinal anaesthesia
the blood volume pumped by the heart at each stroke
Secondary outcomes
-
Arterial blood pressure mmHg and change from baseline
Time frame: 0-45 minutes after spinal anaesthesia
mmHg measured by arterial catheter
Sponsors and collaborators
Lead sponsor
Karolinska Institutet
Other
Registry information
Official study title
Is Postspinal Hypotension a Sign of Impaired Cardiac Performance in the Elderly? An Observational Mechanistic Study
Important dates
- Study start
- 2012
- Primary completion
- 2014
- Study completion
- 2014
- First posted
- Nov 30, 2016
- Registry last updated
- Sep 18, 2020
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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