Status:

COMPLETED

The Role of Oxygen in the Management of Dyspnoea in Advanced Cancer

Lead Sponsor:

Bayside Health

Collaborating Sponsors:

Peter MacCallum Cancer Centre, Australia

Bethlehem Griffiths Research Foundation

Conditions:

Cancer

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

The purpose of this study is to determine the effect that oxygen has when administered to patients complaining of shortness of breath, where the underlying cause of this symptom is advanced cancer. Th...

Detailed Description

Dyspnoea is a devastating symptom in patients with advanced cancer. Management strategies are limited and include behavioural therapies such as relaxation, and pharmacological therapies such as opioid...

Eligibility Criteria

Inclusion

  • Patients who have dyspnoea mainly due to advanced cancer. Patients with a history of COAD will be eligible for participation in this study as long as the main mechanism of current dyspnoea is related to tumor.
  • intensity of dyspnoea of at least 3 on a 0-10 visual analogue scale at the time of treatment.
  • Regular Bronchodilators and corticosteroids and other adjuvant medications for dyspnoea will be allowed to continue during the study. Inhaled bronchodilator steriods may not be used during the study period.
  • Patients may be receiving regular oral or parenteral opioids and opioid dose must be stable for 24 hours.
  • Patients must have normal cognitive status defined as normal state of arousal and absence of obvious clinical findings of confusion, memory or concentration deficit according to Blessed Orientation Memory \& Concentration mental status examination (score\<10).
  • Patients must be 18 years of age or older.
  • Patients must have no contraindications to oxygen.
  • Patients must sign written informed consent.

Exclusion

  • Patients who have evidence of acute respiratory distress.
  • Patients who are currently oxygen dependent
  • Patients who refuse to participate or are deemed incapable of completing the research.

Key Trial Info

Start Date :

November 1 2000

Trial Type :

INTERVENTIONAL

End Date :

March 1 2005

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT00206609

Start Date

November 1 2000

End Date

March 1 2005

Last Update

September 21 2005

Active Locations (1)

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Page 1 of 1 (1 locations)

1

The Alfred Hospital

Prahran, Victoria, Australia, 3004