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Effect of hemodynamic management guided by P[v-a]CO2 on the quality of recovery after thoracoscopic lobectomy

Effect of hemodynamic management guided by P[v-a]CO2 on the quality of recovery after thoracoscopic lobectomy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098400
Enrollment
Unknown
Registered
2025-03-07
Start date
2024-12-12
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Lung cancer

Interventions

Usual care group (GroupC):The management goals of group C were MAP > 65mmHg (adjusted to no more than ±20% fluctuation before anesthesia for hypertensive patients), urine output > 0.5ml/kg/h, lactate
P[v-a]CO2 group (group P):The goal of group P management is to infuse HES 250ml (if PPV>13) or norepinephrine 0.01~0.1µg/kg/min (if PPV75% and P[v-a]CO2>6mmHg). If SCvO2 95% and Hb is suitable, P[v-a]

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients undergoing elective thoracoscopic lobectomy Age >= 18 years old ASA Grading I.~III Voluntarily signed informed consent

Exclusion criteria

Exclusion criteria: Abnormal preoperative lung function (FEV1= 13 points; Patients with renal insufficiency (serum creatinine and urea nitrogen more than 1.2 times the normal range) or abnormal liver function, AST/ALT greater than 1/5/2 times the normal value; maximum vital capacity (FVC) 30kg/m^2 Allergy to hydroxyethyl starch History of upper respiratory tract or pulmonary infection within the past 4 weeks Severe pleural effusion and atelectasis before surgery Patient refuses to participate in the study

Design outcomes

Primary

MeasureTime frame
Postoperative recovery quality;

Countries

China

Contacts

Public ContactSun Defeng

The First Affiliated Hospital of Dalian Medical University

sdf-yl@163.com+86 180 9887 6191

Outcome results

None listed

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