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The effect of optimised rehydration guided by volume responsiveness on hypertension after induction of general anaesthesia in elderly debilitated patients

The effect of optimised rehydration guided by volume responsiveness on hypertension after induction of general anaesthesia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095294
Enrollment
Unknown
Registered
2025-01-06
Start date
2025-01-15
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

Hypotension after induction of general anesthesia

Interventions

Experimental group:Fluid responsiveness test was performed before induction of general anesthesia. Patients with positive fluid responsiveness were given 8ml/kg colloid supplement, and those with nega
Control group:General anesthesia was performed according to the usual procedure without additional intervention

Sponsors

Shanghai Jiaotong University School of Medicine Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=65 years old; 2. RAI-C score > 15; 3. ASA grade 1-3; 4.For patients undergoing elective surgery with preoperative gastrointestinal preparation, the expected operation time is more than 2 hours; 5. signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Venous filling ultrasound score (VExUS) >= 1 point; 2. previous history of cardiac surgery, such as coronary artery bypass grafting, valve replacement surgery, etc; 3. patients with persistent atrial fibrillation or moderate to severe valvular regurgitation or moderate to severe valvular regurgitation; 4.Patients with moderate to severe pulmonary hypertension or combined with moderate or severe pleural effusion; 5. patients with massive ascites; 6. Inability to communicate before surgery (coma, speech disorders, etc.); 7. Severe hepatic and renal dysfunction (Child-Pugh class C/ preoperative dialysis); 8. Patients with endocrine hypertension (e.g., pheochromocytoma); 9. Insufficient ultrasound window or history of allergy to ultrasound coupler; 10. History of succinylated gelatin-related allergy.

Design outcomes

Primary

MeasureTime frame
Incidence of hypotension within 15 minutes after induction of anesthesia;Accuracy of novel non-invasive ultrasound in predicting fluid responsiveness;

Secondary

MeasureTime frame
Doses of vasoactive drugs were used during the procedure;The incidence of vomiting within 48 hours after surgery;The number and duration of intraoperative hypotension;Incidence of postoperative adverse events;All-cause mortality at 30 days after surgery;The rate of creatinine change at 72 hours after operation;Dosage of vasoactive agents within 15 min after induction of anesthesia;Intraoperative fluid balance;Fluid balance was achieved 24 hours after surgery;

Countries

China

Contacts

Public ContactQuanhong Zhou

Shanghai Jiaotong University School of Medicine Affiliated Sixth People's Hospital

zhouanny@hotmail.com+86 137 6144 1463

Outcome results

None listed

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