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Clinical Study on Preoperative Echocardiographic Parameters for Predicting Hypotension After General Anesthesia Induction

Clinical Study on Preoperative Echocardiographic Parameters for Predicting Hypotension After General Anesthesia Induction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124237
Enrollment
Unknown
Registered
2026-05-09
Start date
2026-05-10
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Hypotension after general anesthesia induction

Interventions

The group of patients who underwent laparoscopic surgery:None

Sponsors

Second Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–65 years, willing to participate in this study, and able to provide written informed consent; 2. ASA physical status I–III; 3. Conscious and alert; 4. Sinus rhythm; 5. Patients whose electrocardiogram collection, left ventricular outflow tract velocity-time integral measurement sites, and inferior vena cava collection sites are not covered with gauze or bandages.

Exclusion criteria

Exclusion criteria: 1. Difficult airway management or intubation; 2. Baseline mean arterial pressure (MAP) below 70 mmHg; 3. Non-sinus rhythm, stroke, mental disorders, peripheral vascular disease, or presence of an implanted pacemaker or cardioverter-defibrillator; 4. Long-term use of angiotensin-converting enzyme inhibitors (ACEIs) / angiotensin receptor blockers (ARBs); 5. Severe heart disease, unstable angina, or ejection fraction below 40%

Design outcomes

Primary

MeasureTime frame
Baseline characteristics (including gender, age, body mass index, ASA class, preoperative Hb, pre-anesthesia fasting time and fluid volume,comorbidities [hypertension,diabetes],baseline systolic blood pressure, diastolic blood pressure, mean arterial pressure,heart rate);Anesthesia-related data (including baseline LVOT-VTI, PI, SBP, DBP, MAP, HR, intraoperative dosages of etomidate, sufentanil, and rocuronium, as well as post-anesthesia hemodynamic data).;

Countries

China

Contacts

Public ContactQiao Jingwen

Second Hospital of Shanxi Medical University

feibusita@sxmu.edu.cn+86 152 3404 4085

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026