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Non-Invasive Ventilation in Terminally Ill Cancer Patients
This study is currently recruiting participants.
Verified by Fondazione Salvatore Maugeri, April 2009
First Received: September 20, 2007   Last Updated: April 10, 2009   History of Changes
Sponsored by: Fondazione Salvatore Maugeri
Information provided by: Fondazione Salvatore Maugeri
ClinicalTrials.gov Identifier: NCT00533143
  Purpose

The occurrence of acute respiratory failure (ARF) is often seen by oncologists as a terminal phase of the disease, this view being based on studies reporting limited survival at considerable costs in such patients. A large proportion of cancer patients with severe respiratory failure are denied admission to an ICU because intensive care specialists are aware that intubation and mechanical ventilation are both strong predictors of mortality in critically ill cancer patients. This holds particularly true in the subset of patients who are not receiving chemotherapy or radiotherapy because of the advanced stage of their disease, and who are also not affected by an episode of ARF, related to a reversible cause. These patients often receive oxygen therapy and morphine in an attempt to improve oxygenation and/or relieve the ensuing dyspnea. Non-invasive mechanical ventilation (NIV) is now the first line treatment of ARF in selected populations (e.g., those with COPD) and has been used sporadically as a potential treatment of acute respiratory failure in patients with a "do-not-intubate" order. The International Consensus Conference on Intensive Care Medicine stated that "the use of NIV may be justified in selected patients who are "not to be intubated" and may provide patient comfort and facilitate physician-patient interaction." "Early" NIV has been successfully used so far in cancer patients only to prevent intubation among those with hematologic malignancies, while a pilot study has assessed the feasibility of NIV also as a "palliative" treatment of end-stage solid cancer patients. So far we are lacking data about the "pure palliative" effects of NIV,in patients with end-stage solid cancer.

The aim of this multicenter randomised study will be to evaluate on a large scale the feasibility, clinical efficacy and impact on quality of life and dyspnea of NIV versus standard medical in patients with respiratory failure, not related to a reversible cause, and solid cancer needing palliative care treatment.


Condition Intervention Phase
Cancer
Other: non invasive ventilation (NIV)
Phase IV

Study Type: Interventional
Study Design: Supportive Care, Randomized, Single Blind (Investigator), Active Control, Parallel Assignment, Efficacy Study
Official Title: Multicenter, Randomised Study of the Use of Non-Invasive Ventilation (NIV) Versus Oxygen Therapy (O2) in Reducing Dyspnea in End-Stage Solid Cancer Patients With Respiratory Failure and Distress

Resource links provided by NLM:


Further study details as provided by Fondazione Salvatore Maugeri:

Primary Outcome Measures:
  • dyspnea [ Time Frame: 48 hours ] [ Designated as safety issue: No ]
  • morphine dosage [ Time Frame: 48 hours ] [ Designated as safety issue: No ]
  • Quality of Life [ Time Frame: 48 hours ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Arterial Blood Gases [ Time Frame: 48 hours ] [ Designated as safety issue: No ]
  • Survival [ Time Frame: 48 hours ] [ Designated as safety issue: No ]

Estimated Enrollment: 200
Study Start Date: September 2007
Estimated Study Completion Date: December 2009
Estimated Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
2: Experimental
Non-invasive ventilation
Other: non invasive ventilation (NIV)
NIV is a form of mechanical ventilation delivered through a face or nasal mask and therefore not requiring endotracheal intubation. It will be delivered according to the compliance and tolerance of the patients.

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Major criteria for enrollment into the study were one of the following:

  • PaO2/FiO2 ratio < 250 + one of the two following:

    • dyspnea with recruitment of the accessory muscles and/or abdominal muscles recruitment; and
    • respiratory rate > 30 b/ min. Hypercapnia per se is not a criteria of inclusion, but it is not an exclusion criteria if chronic.

Exclusion Criteria:

  • Potentially reversible causes of exacerbation such as (CPE, pneumonia or exacerbation of chronic pulmonary disorders) coma
  • Refusal of treatment
  • Inability to protect the airways
  • An agitated or uncooperative patient
  • Anatomical abnormalities interfering with mask fit
  • Uncontrolled cardiac ischemia or arrhythmias
  • Failure of more than two organs
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00533143

Contacts
Contact: Stefano Nava, MD 39 0382 5921 ext 2806 snava@fsm.it

Locations
Italy
Istituto Scientifico di Pavia, Salvatore Maugeri Foundation Recruiting
Pavia, Italy, 27100
Contact: Stefano Nava, MD     39 0382 5921 ext 2806     snava@fsm.it    
Principal Investigator: Stefano Nava, MD            
Sponsors and Collaborators
Fondazione Salvatore Maugeri
Investigators
Principal Investigator: Stefano Nava Fondazione S.Maugeri
  More Information

No publications provided

Responsible Party: Fondazione S.Maugeri ( Principal investigator )
Study ID Numbers: 322 CEC
Study First Received: September 20, 2007
Last Updated: April 10, 2009
ClinicalTrials.gov Identifier: NCT00533143     History of Changes
Health Authority: Italy: Ethics Committee

Keywords provided by Fondazione Salvatore Maugeri:
Solid cancer patient
Non-invasive ventilation
Acute Respiratory Failure

Study placed in the following topic categories:
Respiratory Insufficiency
Respiratory Tract Diseases
Respiration Disorders
Dyspnea

Additional relevant MeSH terms:
Respiratory Insufficiency
Respiratory Tract Diseases
Respiration Disorders

ClinicalTrials.gov processed this record on September 10, 2009