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Effect of continuous infusion of phenylephrine during induction on volume responsiveness in elderly patients

Effect of continuous infusion of phenylephrine during induction on volume responsiveness in elderly patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042844
Enrollment
Unknown
Registered
2021-01-30
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-05-17

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

Conditions

shock

Interventions

Experimental group:After endotracheal intubation for 5 minutes, it begins to infuse phenylephrine of 0.2 µg/kg/min for 5 minutes, and then 5ml/kg ideal body weight of Sodium Lactate Ringer's Injectio
control group:After endotracheal intubation for 5 minutes, it begins to infuse saline solution at the corresponding rate with phenylephrine of 0.2 µg/kg/min for 5 minutes, and then 5ml/kg ideal body w

Sponsors

Department of Anesthesiology, Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who have selective operation under general anesthesia with mechanical ventilation for more than 2 hours; 2. Age 65 and above, gender is not limited; 3. The ASA class I, II, III; 4. Heart function grade of NYHA I, II, systolic blood pressure < 180 mmHg, diastolic pressure < 110 mmHg; 5. 18.5 kg / ? <= BMI < 27.9 kg / ?; 6. Patients who are willing to cooperate with this study, understand and voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Presence of hypertension grade 3 (very high risk), severe arrhythmia, severe heart valve disease, left ventricular ejection fraction < 50%; 2. There are contraindications of central venous catheterization or radial artery catheterization; 3. The patient had a pulmonary infection two weeks before surgery or severe pulmonary disease or a history of lobotomy; 4. Other serious organ dysfunction, such as liver function Child grade C, uremia; 5. For other reasons, the investigator considers it inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
stroke volume index;

Secondary

MeasureTime frame
stroke volume variation;pulse pressure variation;

Countries

China

Contacts

Public ContactHongfei Zhang

Department of Anesthesiology, Zhujiang Hospital of Southern Medical University

zhanghongfei@smu.edu.cn+86 20-61643299

Outcome results

None listed

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