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Clinical Trials/NCT01217151
NCT01217151
Completed
N/A

Perioperative Hemodynamic Goal-directed Optimization Using the Noninvasive NICOM™ Monitoring Device in Major Abdominal Surgery

Hospital Universitario La Paz4 sites in 2 countries142 target enrollmentJanuary 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Major Abdominal Surgery
Sponsor
Hospital Universitario La Paz
Enrollment
142
Locations
4
Primary Endpoint
Decrease in hospital length of stay
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

In the last years, there is a growing interest in the improvement of prognosis and shortening of hospital length of stay in high-risk surgical patients. Several evidence-based protocols ("fast-track" surgery) have been developed and implemented in some hospitals for this purpose. Cardiovascular optimization through the so-called "goal-directed therapy" (GDT) is a key element in these protocols. Previous studies in the literature use invasive monitors to assess hemodynamics. The NICOM ™ is a non-invasive monitor validated in several clinical scenarios. The aim of the present randomized, international, multi-center, open-label clinical trial is to use a GDT protocol (including colloid boluses and vasoactive drug infusion) based on data obtained from the NICOM™ device (cardiac index and mean arterial pressure) to test the hypothesis that GDT is superior to standard practice in terms of reduction in the incidence of perioperative complications and length of hospital stay in high-risk major abdominal surgery patients (requiring ICU surveillance for, at least, 24 hours). As secondary objectives, time to first flatus, wound infection, anastomotic leaks and mortality will be analysed. All patients will be followed from the day of surgery up to hospital discharge (determined by a specialist surgeon not involved in the study) or death.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
November 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Adult patients scheduled for:
  • Open colorectal surgery: hemicolectomy, pancolectomy, abdomino-perineal resection.
  • Gastrectomy.
  • Small bowel resection.
  • Signed written informed consent.

Exclusion Criteria

  • Less than 18 years old.
  • Laparoscopic procedure.
  • Emergency surgery.
  • Intra-abdominal infection.
  • Patients not requiring ICU admission (patients should stay for at least the first day at the ICU).
  • Life expectancy lower than 60 days.
  • Disseminated malignancy.

Outcomes

Primary Outcomes

Decrease in hospital length of stay

Time Frame: Three months

Secondary Outcomes

  • Incidence of wound infection(Three weeks)
  • Time to peristalsis recovery(Three weeks)
  • Incidence of anastomotic leaks(Three weeks)
  • Any cause mortality(Three months)

Study Sites (4)

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