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Effect of SVV Guided Fluid Therapy on Blood Loss and Postoperative Outcomes

A

Asan Medical Center

Status

Completed

Conditions

Bladder Cancer

Treatments

Other: mannitol
Other: crystalloid
Other: colloid
Other: lasix

Study type

Interventional

Funder types

Other

Identifiers

NCT02373735
S2014-2192

Details and patient eligibility

About

The purpose of this study is to investigate the effect of stroke volume variation (SVV) guided fluid therapy on the blood loss and postoperative outcomes in radical cystectomy.

Full description

The purpose of this study is to investigate the effect of stroke volume variation(SVV) guided fluid therapy on the blood loss and postoperative outcomes in radical cystectomy. Patients were randomized to fluid management to maintain <10% SVV (group A), or to undergo fluid management during radical cystectomy to maintain SVV 10-20% (group B). Intraoperative blood loss and hemodynamic parameters, perioperative laboratory data, and postoperative complications were compared between two groups.

Enrollment

64 patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Bladder cancer patients who received radical cystectomy
  • Patients with American Society of Anesthesiologists physical status scale classification 1, 2
  • Patients who agree with written informed consent

Exclusion criteria

  • Patients with history of arrhythmia, heart failure patients
  • Patients with history of renal failure patients
  • Patients with history of abdominal surgery
  • Patients who received emergency operation
  • Patients who do not agree with study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

64 participants in 2 patient groups

Group A (SVV <10% group)
Active Comparator group
Description:
* infuse crystalloid (Hartmann's solution) 6-10 ml/kg/hr continuously during surgery * infuse colloid (Volulyte) 200 ml if SVV is ≥ 10% during the surgery Interventions: crystalloid (Hartmann's solution), colloid (Volulyte)
Treatment:
Other: crystalloid
Other: colloid
Group B (SVV 10-20% group)
Experimental group
Description:
* infuse crystalloid (Hartmann's solution) 2-4 ml/kg/hr until cystectomy, 6-10 ml/kg/hr after cystectomy * infuse colloid (Volulyte) 200 ml if SVV is \> 20% * infuse mannitol 0.5 g/kg or lasix 5 mg if SVV \< 10% Interventions: crystalloid (Hartmann's solution), colloid (Volulyte), mannitol, lasix
Treatment:
Other: lasix
Other: crystalloid
Other: mannitol
Other: colloid

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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