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Effect of corrected left ventricular-ejection time guided perioperative fluid therapy on preventing hypotension after general anesthesia induction in elderly patients

Effect of corrected left ventricular-ejection time guided perioperative fluid therapy on preventing hypotension after general anesthesia induction in elderly patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090252
Enrollment
Unknown
Registered
2024-09-26
Start date
2024-10-08
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Hypotension after general anesthesia.

Interventions

Part 1: Corrected left ventricular-ejection time prediction for elderly patients with hypotension after induction of general anesthesia group:Corrected left ventricular-ejection time
Part 2: Corrected left ventricular-ejection time guided perioperative fluid therapy group:Corrected left ventricular-ejection time guided perioperative fluid therapy
Part 2: Routine perioperative fluid therapy group:Routine perioperative fluid therapy

Sponsors

Beijing Chao-Yang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Age ranges from 60-85 years old. 2.Scheduled for elective non-cardiac surgery. 3.ASA (American Society of Anesthesiologists) grade I-III classification. 4.Undergoing general anesthesia with endotracheal intubation or/and laryngeal mask airway insertion. 5.Willingness to participate in this study and providing the informed consent.

Exclusion criteria

Exclusion criteria: 1.Poor impedance cardiogram (ICG) waveform caused by obvious interference (such as agitation, coughing, shivering, limb shaking). 2.Poorly controlled hypertension (mean arterial pressure > 130mmHg or systolic blood pressure> 180 or diastolic blood pressure> 110 mmHg for noninvasive or invasive blood pressure after 5 minutes of rest in the preoperative waiting area or in the operation room. 3.Skin rashes, infections, or ulcers at the site where the electrodes of the chest impedance monitoring device to be attached. 4.Severe aortic insufficiency. 5.Atrial septal defect or ventricular septal defect. 6.Severe aortic sclerosis or post-aortic repair surgery. 7.Aortic aneurysm or aortic dissection. 8.Status post-pacemaker implantation. 9.Height below 120cm or above 230cm. 10.Weight less than 30kg or more than 155kg. 11.BMI greater than 30 kg/m2 or less than 15 kg/m2. 12.History of allergies or other serious adverse reactions to the drugs used in the study. 13.History of allergies to medical tape, electrocardiogram electrodes, and medical skin surface dressings involved in this study.

Design outcomes

Primary

MeasureTime frame
Part 1: The area under the ROC curve and optimal threshold of corrected left ventricular-ejection time for predicting hypotension after general anesthesia induction in elderly patients;Part 2: Incidence of hypotension after general anesthesia induction;

Secondary

MeasureTime frame
Part 1: Incidence of hypotension after general anesthesia induction;Part 1: Patient satisfaction 24 hours after surgery;Part 1: Incidence of skin allergy with electrode of non-invasive hemodynamic detector;Part 2: Hemodynamic changes before and after fluid therapy and induction;Part 2: Patient satisfaction 24 hours after surgery;Part 2: Incidence of skin allergy with electrode of non-invasive hemodynamic detector;

Countries

China

Contacts

Public ContactAnshi Wu

Beijing Chao-Yang Hospital, Capital Medical University

wuanshi88@163.com+86 10 85231325

Outcome results

None listed

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