CHEST - Pilot Study CPAP: Heliox Effects on Stability and Therapeutics
| ISRCTN | ISRCTN82423314 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN82423314 |
| Protocol serial number | AL001 |
| Sponsor | Imperial College London (UK) |
| Funder | Gas will be provided by BOC Ltd. Equipment and application fees will be provided by Viasys |
- Submission date
- 19/07/2005
- Registration date
- 21/09/2005
- Last edited
- 04/01/2011
- Recruitment status
- Stopped
- Overall study status
- Stopped
- Condition category
- Respiratory
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Parviz Habibi
Scientific
Scientific
Imperial College London
Norfolk Place
London
W21PG
United Kingdom
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study acronym | CHEST |
| Study objectives | Heliox + oxygen driven continuous positive airway pressure (CPAP) reduces work of breathing and improves oxygenation and carbon dioxide clearance more than air + oxygen driven CPAP |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Respiratory distress requiring CPAP |
| Intervention | Heliox + oxygen driven continuous positive airway pressure (CPAP) versus air + oxygen driven CPAP. |
| Intervention type | Other |
| Primary outcome measure(s) |
Work of breathing |
| Key secondary outcome measure(s) |
Oxygenation, carbon dioxide clearance |
| Completion date | 01/03/2007 |
| Reason abandoned (if study stopped) | Lack of funding |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Child |
| Upper age limit | 1 Year |
| Sex | All |
| Target sample size at registration | 20 |
| Key inclusion criteria | Children under 1 year of age with respiratory distress requiring CPAP |
| Key exclusion criteria | Refusing consent, pneumothorax, FiO2 >0.6, imminent intubation, respiratory failure |
| Date of first enrolment | 01/09/2005 |
| Date of final enrolment | 01/03/2007 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Imperial College London
London
W21PG
United Kingdom
W21PG
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |