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Ultrasound of the Inferior Vena Cava in the Prevention of Hypotension After Induction of General Anesthesia

Multidimensional Ultrasound of the Inferior Vena Cava in the Prevention of Hypotension After Induction of General Anesthesia

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06530901
Enrollment
100
Registered
2024-07-31
Start date
2024-09-01
Completion date
2025-03-31
Last updated
2024-08-05

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

Conditions

Elderly Patients Undergoing Elective Non-cardiac Surgery

Keywords

hypotension, general anesthesia, inferior vena cava

Brief summary

Based on the preoperative ultrasound detection of various parametric indicators of the inferior vena cava cross-section, including the ratio of the inferior vena cava's long and short axes, cross-sectional area and circumference during two-dimensional and three-dimensional imaging, as well as the changes in respiratory variability of each parameter, we explored the predictive value of IVC ultrasound indicator parameters on hypotension after induction of general anesthesia in elderly patients undergoing elective non-cardiac surgery, screened the sensitive indicators, and calculated the cut-off values.

Interventions

DIAGNOSTIC_TESTMultidimensional ultrasound of the inferior vena cava

Cross-sectional parameters of the inferior vena cava include two-dimensional longitudinal diameter, cross-sectional length and short diameter, circumference, and cross-sectional area, as well as cross-sectional length and short diameter, circumference, and cross-sectional area in three-dimensional imaging

Sponsors

Zhuan Zhang
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Elderly patients undergoing elective non-cardiac surgery under general anesthesia; * Age 65-85 years old; * Body mass index (BMI) 18-28 kg/m2; * American society of anesthesiologists (ASA) class I-III.

Exclusion criteria

* Patient refusal or lack of cooperation; * Inability to communicate properly; * Severe sinus bradycardia, pacemaker implantation, atrioventricular block, and atrial fibrillation; * Presence of severe hepatic and renal function abnormalities; * Preoperative cardiac ultrasound suggesting LVEF \<50%; * Tricuspid valve displacement \<16 mm by preoperative cardiac ultrasound; * Chronic obstructive pulmonary disease; * Pulmonary hypertension; * Administration of drugs that inhibit the renin-angiotensin-aldosterone system; * Possibility of a difficult airway.

Design outcomes

Primary

MeasureTime frameDescription
Changes in the level of Mean Arterial PressureBaseline (before induction), 10 min after inductionThe outcome above should be measured at the time before induction, 1 min after induction, 2 min after induction, 3 min after induction, 4 min after induction, 5 min after induction,10 min after induction
Changes in the level of Systolic Blood PressureBaseline (before induction), 10 min after inductionThe outcome above should be measured at the time before induction, 1 min after induction, 2 min after induction, 3 min after induction, 4 min after induction, 5 min after induction,10 min after induction
Multidimensional ultrasound of the inferior vena cavaBaseline (before induction)The outcome above should be measured at the time before induction

Secondary

MeasureTime frameDescription
Changes in the level of Heart RateBaseline (before induction), 10 min after inductionThe outcome above should be measured at the time before induction, 1 min after induction, 2 min after induction, 3 min after induction, 4 min after induction, 5 min after induction,10 min after induction
Changes in the level of Diastolic Blood PressureBaseline (before induction), 10 min after inductionThe outcome above should be measured at the time before induction, 1 min after induction, 2 min after induction, 3 min after induction, 4 min after induction, 5 min after induction,10 min after induction

Countries

China

Contacts

Primary Contactzhuan zhang, professor
zhangzhuancg@163.com+8615062791355

Outcome results

None listed

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