Which method of pain relief is most effective for chest drain removal in postoperative cardiac patients?
ISRCTN | ISRCTN36538293 |
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DOI | https://doi.org/10.1186/ISRCTN36538293 |
Secondary identifying numbers | N0054119937 |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 17/12/2008
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Signs and Symptoms
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr M Akrofi
Scientific
Scientific
Department of Anaesthesia
The Cardiothoracic Centre
Liverpool NHS Trust
Thomas Drive
Liverpool
L14 3PE
United Kingdom
Phone | +44 (0)151 228 1616 |
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Study information
Study design | Randomised controlled trial |
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Primary study design | Interventional |
Secondary study design | Randomised controlled trial |
Study setting(s) | Not specified |
Study type | Not Specified |
Scientific title | |
Study objectives | Which of the currently available methods (entonox, intravenous morphine, subcutaneous bupivacaine) used for the control of analgesia during chest drain removal is most effective? |
Ethics approval(s) | Not provided at time of registration |
Health condition(s) or problem(s) studied | Signs and Symptoms: Pain |
Intervention | Patients randomised to 50% entonox, 100 mcg/kg morphine and 0.5% bupivacaine. |
Intervention type | Other |
Primary outcome measure | 1. Pain scores after chest drain removal assessed by the short form McGill questionnaire 2. Effect of anaesthetic agent on length of intensive care unit stay |
Secondary outcome measures | Not provided at time of registration |
Overall study start date | 15/07/2002 |
Completion date | 15/07/2003 |
Eligibility
Participant type(s) | Patient |
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Age group | Not Specified |
Sex | Not Specified |
Target number of participants | 66 |
Key inclusion criteria | 66 patients receiving chest drain removal following major cardiac surgery. |
Key exclusion criteria | Not provided at time of registration |
Date of first enrolment | 15/07/2002 |
Date of final enrolment | 15/07/2003 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Department of Anaesthesia
Liverpool
L14 3PE
United Kingdom
L14 3PE
United Kingdom
Sponsor information
Department of Health (UK)
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
Website | http://www.doh.gov.uk |
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Funders
Funder type
Government
The Cardiothoracic Centre Liverpool NHS Trust (UK)
No information available
Results and Publications
Intention to publish date | |
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Individual participant data (IPD) Intention to share | No |
IPD sharing plan summary | Not provided at time of registration |
Publication and dissemination plan | Not provided at time of registration |
IPD sharing plan |
Study outputs
Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
---|---|---|---|---|---|
Results article | results | 01/01/2005 | Yes | No |