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The Effect of Intraoperative Goal-directed Fluid Therapy on Postoperative Outcomes of Patients Undergoing Lobectomy Operations

The Effect of Intraoperative Goal-directed Fluid Therapy on Postoperative Outcomes of Patients Undergoing Lobectomy Operations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17011665
Enrollment
Unknown
Registered
2017-06-14
Start date
2017-07-01
Completion date
Unknown
Last updated
2017-06-19

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

Conditions

Intraoperative fluid management

Interventions

Group G: Goal-directed Fluid Therapy
Group C:Restrictive Fluid Therapy

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Approved by the hospital Ethics Committee and signed informed consent; (2) Patients undergoing elective lobectomy operations; (3) Aged from 18 to 80 years; (4) American Society of Anaesthesiologists physical status from 1 to 3; (5) BMI<28

Exclusion criteria

Exclusion criteria: 1. Severe oesophageal disease; 2. Recent oesophageal or upper airway surgery; 3. Moderate or severe aortic valve disease; 4. Severe functional heart, lung, brain, liver or kidney disease; 5. Severe arrhythmia; 6. Cognitive impairment; 7. Patient rejection.

Design outcomes

Primary

MeasureTime frame
Postoperative complications;

Secondary

MeasureTime frame
Length of stay;Hospital mortality;

Countries

China

Contacts

Public ContactJie Zhang

The First Affiliated Hospital of Zhengzhou University

joannyzh@163.com+86 13703939292

Outcome results

None listed

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