A prospective blinded randomised controlled trial investigating the use of patient-controlled intravenous analgesia compared with nurse-controlled anaesthesia following first time coronary artery bypass surgery.
| ISRCTN | ISRCTN80168835 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN80168835 |
| Secondary identifying numbers | N0201139523 |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 18/07/2016
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
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 David Royston
Scientific
Scientific
Anaesthetics
Royal Brompton & Harefield NHS Trust
Harefield Hospital
Hill End Road
Harefield
UB9 6JH
United Kingdom
| Phone | +44 (0)1895 823737 |
|---|---|
| D.Royston@rbh.nthames.nhs.uk |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Participant information sheet | Not available in web format, please use contact details to request a participant information sheet |
| Scientific title | A prospective blinded randomised controlled trial investigating the use of patient-controlled intravenous analgesia compared with nurse-controlled anaesthesia following first time coronary artery bypass surgery. |
| Study objectives | Is more analgesia used in patient controlled or nurse controlled regimes? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Post-operative pain |
| Intervention | Patient-controlled intravenous analgesia compared with nurse-controlled anaesthesia |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/06/2003 |
| Completion date | 31/05/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | Not provided at time of registration |
| Key inclusion criteria | Patients undergoing first time coronary artery bypass surgery |
| Key exclusion criteria | Does not match inclusion criteria |
| Date of first enrolment | 01/06/2003 |
| Date of final enrolment | 31/05/2004 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Royal Brompton & Harefield NHS Trust
Harefield
UB9 6JH
United Kingdom
UB9 6JH
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.dh.gov.uk/Home/fs/en |
|---|
Funders
Funder type
Government
Royal Brompton and Harefield NHS Trust (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| 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 |
Editorial Notes
18/07/2016: No publications found, verifying study status with principal investigator.
