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Goal-directed Intraoperative Fluid Therapy in High-risk Surgery

NCT02470221 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2019-05-31

No results posted yet for this study

Summary

This study is aim to assess the effect of goal-directed intraoperative fluid therapy on patient's postoperative incidence rates of complications, length of hospitalization and hospitalization cost.

This is an observational study followed cohort study design, due to the two therapies were not randomized assigned to the two cohorts. The details are described as follow.

Conditions

  • Postoperative Complications
  • Fluid Overload

Interventions

OTHER

Applying goal-directed fluid therapy by continuous hemodynamic monitoring system

Applying continuous hemodynamic monitoring system ( Vigileo/Flotrac) to monitor Stroke Volume Variation and Cardiac Output and further manage intra-operative fluid therapy.

OTHER

Conventional fluid therapy

Applying conventional fluid therapy according to Peking Union Medical College Hospital standard.

Sponsors & Collaborators

  • Huang YuGuang

    lead OTHER

Principal Investigators

  • Yuguang Huang, MD · Peking Union Medical College Hospital

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-01
Primary Completion
2018-02-10
Completion
2018-07-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02470221 on ClinicalTrials.gov