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OpenTrials
Completed

NCT Number: NCT01217151

Perioperative Hemodynamic Optimization Using the NICOM Device

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.

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Carmel Medical Center, Haifa, Israel

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Hemodynamic Monitoring

Device

Hemodynamic monitoring based on the NICOM device

Usual treatment

Other

Hemodynamic monitoring based on common practice

Primary outcomes

  1. Decrease in hospital length of stay

    Time frame: Three months

Secondary outcomes

  1. Time to peristalsis recovery

    Time frame: Three weeks

    Peristalsis shall be assessed by first flatus after abdominal surgery

  2. Incidence of wound infection

    Time frame: Three weeks

  3. Incidence of anastomotic leaks

    Time frame: Three weeks

  4. Any cause mortality

    Time frame: Three months

Sponsors and collaborators

Lead sponsor

Hospital Universitario La Paz

Other

Collaborators

  • Carmel Medical Center
  • Hospital General de Ciudad Real
  • Hospital del Rio Hortega
  • University Hospital of the Nuestra Señora de Candelaria
  • University of Valencia

Registry information

Official study title

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

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Oct 8, 2010
Registry last updated
Nov 20, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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