NCT Number: NCT00230984
IRAD2 : Patients With Respiratory Failure at Home
Title : Effects of home pulmonary rehabilitation in patients with chronic respiratory failure and nutritional depletion.
This is a randomized controlled, open clinical trial with two groups.
* first group, 100 patients : control group, patients followed with no add-on intervention * Second group, 100 patients : rehabilitation group with education, oral supplements, exercise and androgenic steroids.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
University Hospital Dominique Larrey, Limoges, France
About this study
Title : Effects of home pulmonary rehabilitation in patients with chronic respiratory failure and nutritional depletion
State of the art :
The IRAD2 trial is evaluating a 3-month home intervention which includes education, oral supplements, exercise and androgenic steroids in undernourished patients with chronic respiratory failure. The main objective is to increase the six-minute walking distance by more than 50 m with an improvement in health-related quality-of-life. Secondary end-points include a reduction in exacerbation rates by 25%, a reduction in health-related costs and an increase in survival during the year following intervention.
Material and methods :
This interventional, multi-centre, prospective, two-armed parallel, controlled trial is being conducted in 200 patients. In both groups, "Control" and "Rehabilitation", 7 home visits are scheduled during the 3-month intervention for education purpose. In the "Rehabilitation" group, patients will receive 160 mg/d of oral testosterone undecanoate in men, 80 mg/d in women, oral dietary supplements (563 kcal/d) and exercises on an ergometric bicycle 3 to 5 times a week.
Expected results :
In the event of significant responses to intervention, this trial would validate a comprehensive and global home-care for undernourished patients with chronic respiratory failure combining therapeutic education, oral supplements, androgenic substitution and physical activity.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- well informed and consenting person
- woman is old enough to procreate
- Assisted respiratory treatment at home for 3 months : oxygenotherapy > 8 hours per day and/or assisted ventilation > 6 hours per day.
- PaO2 without oxygenotherapy ≤ 8 kPa or 60 mmHg on ambient air at the beginning of assisted respiratory treatment.
- Affection : chronic obstructive bronchopneumopathy, diffuse bronchial dilatation, non neuromuscular restrictive syndrome (pulmonary diffuse infiltration, parietal lesion) obstructive and restrictive syndrome.
- malnourished person, one of following criteria :Body Mass Index ≤ 21kg/m2 or weight loss (10% of the previous weight) or non-fatty mass measured by 50 Hz impedancemetry ≤25th percentiles or ≤ 63% of ideal weight for women, ≤ 67% of ideal weight for men.
Exclusion criteria
- Sleep apnea with daytime drowsiness (drowsiness scale of Epworth > 9/24)
- Known pathology that reduce the vital prognosis at 6 months (AIDS, cancer...).
- History of hormone dependent cancer ( breast cancer, prostate cancer), pathologic Prostate Specific Antigen.
- Inability to follow a rehabilitation program
Treatment and study plan
Oral dietary supplements (563 kcal/d), RESPIFOR
Drugexercises on an ergometric bicycle 3 to 5 times a week
Behavioral160 mg/d of oral testosterone undecanoate in men, 80 mg/d in women
DrugPrimary outcomes
-
An increase of the six-minute walking distance by more than 50 m with an improvement in health-related quality-of-life.
Secondary outcomes
-
Reduction in exacerbation rates by 25%
-
Quality of life assessed by generic QOL.
-
Reduction in health-related costs
-
Increase in survival during the year following intervention.
Sponsors and collaborators
Lead sponsor
University Hospital, Grenoble
Other
Collaborators
- Association AGIR à Dom,
- Association ANTADIR ,
- Ministry of Health, France
- Nutricia France, swizerland),
- Organon
- Societe Francophone de Nutrition Enterale et Parenterale
Registry information
Official study title
Effects of Home Pulmonary Rehabilitation in Patients With Chronic Respiratory Failure and Nutritional Depletion.
Important dates
- Study start
- 2003
- Primary completion
- 2008
- Study completion
- 2008
- First posted
- Oct 3, 2005
- Registry last updated
- Jul 8, 2009
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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