Clinical Trials Directory

Trials / Completed

CompletedNCT03423888

High-flow Nasal Oxygen in Palliative Care: Pilot Study

Acceptability of High-flow Nasal Oxygen to Relieve Dyspnea in Palliative Care: Pilot Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
University Hospital, Toulouse · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In palliative care, the relief of the dyspnea is necessary. Medications for the reduction of dyspnea have side effects. High-flow nasal cannula oxygen therapy (HFNC) is a new way to deliver oxygen. Investigators hypothesize that HNFC is an acceptable technic for the patient with dyspnea in palliative care. A pilot study with 30 patients will be conducted. Acceptability of HNFC will be studied by the time of use by patients of the HNFC during one week. The effectiveness of HNFC in relieving dyspnea will be studied using Borg scale.

Detailed description

Pilot study for acceptability of high flow nasal cannula oxygen therapy in palliative care Population: 30 patients in palliative care (for lung cancer, terminal respiratory failure) who suffer from dyspnea and have oxygen therapy. Patients with curative care are excluded and patients who require non invasive ventilation. An oral consent is asked. Primary objective: acceptability of HNFC in patients with dyspnea in palliative care during one week Secondary objectives: * Tolerance of HNFC at short term (1h and 24h) and long term (7 days) after initiation of HNFC * Efficiency of HNFC at short term Primary outcome: duration of use of the HNFC during 7 days Secondary outcome: * Tolerance: noise of the system of HNFC, side effects of high flow (nasal dryness..) * Efficiency: evaluation of dyspnea by Borg scale and measure of respiratory rate and saturation of oxygen one hour after initiation of HNFC

Conditions

Interventions

TypeNameDescription
DEVICEhigh-flow nasal cannula oxygen therapy (HNFC)Set up of high-flow nasal oxygen for patient with dyspnea for a respiratory disease without possibility of curative care. Patients who require a treatment by oxygen are included. After 7 days of treatment, acceptability is evaluated by the duration of use of HNFC.

Timeline

Start date
2018-02-13
Primary completion
2022-01-25
Completion
2022-01-25
First posted
2018-02-06
Last updated
2022-04-14

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03423888. Inclusion in this directory is not an endorsement.