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Effects of intraoperative Goal-Directed Fluid Therapy on the perioperative complications following low central venous pressure-assisted liver resection

Effects of intraoperative Goal-Directed Fluid Therapy on the perioperative complications following low central venous pressure-assisted liver resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027017
Enrollment
Unknown
Registered
2019-10-28
Start date
2019-11-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Liver Disease

Interventions

Group 2:Goal-Directed Fluid Therapy(GDFT)
Group 1:Conventional fluid therapy

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients receiving elective lapratomy surgery of liver resecction; 2. Patients aged above 18; ASA I-III; BMI< 30; 3. Receiving general anesthesia combined with TAP.

Exclusion criteria

Exclusion criteria: 1. Patients with AR; 2. Patients with aortic stenosis, peripheral vascular disease etc.; 3. Patients with mental disease or cognitive dysfunction; 4. With history of severe disease such as renal failure, Ischemic heart disease, stroke, cerebral hemorrhage; 5. Patients without informed consent.

Design outcomes

Primary

MeasureTime frame
the incidence of postoperative complications;—

Secondary

MeasureTime frame
postoperative clinical outcomes;length of hospital stay after surgery;readmission rate;—

Countries

China

Contacts

Public ContactJing Cang

Zhongshan Hospital, Fudan University

cangjing_zs@sina.com+86 139 1601 0421

Outcome results

None listed

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