A comparison of subcutaneous morphine and diamorphine given via patient-controlled analgesia after hip replacement
| ISRCTN | ISRCTN49142784 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN49142784 |
| Secondary identifying numbers | N0263048370 |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 05/12/2014
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Signs and Symptoms
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 B Brandner
Scientific
Scientific
Anaesthetics Department
Middlesex Hospital
Mortimer Street
London
W1N 8AA
United Kingdom
| Phone | +44 (0)20 7636 8333 |
|---|---|
| abc@email.com |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Scientific title | A comparison of subcutaneous morphine and diamorphine given via patient-controlled analgesia after hip replacement |
| Study objectives | Is diamorphine better for the patient in terms of pain scores, side effects and feeling of well being? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Pain |
| Intervention | 1. Subcutaneous morphine 2. Diamorphine |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Morphine and diamorphine |
| Primary outcome measure | Subjective visual analogue scores for pain, nausea, sedation and euphoria. |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 30/03/1999 |
| Completion date | 01/09/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 40 patients from Orthopaedic Surgery |
| Key inclusion criteria | Not provided at time of registration |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 30/03/1999 |
| Date of final enrolment | 01/09/2004 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Middlesex Hospital
London
W1N 8AA
United Kingdom
W1N 8AA
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 |
|---|
Funders
Funder type
Hospital/treatment centre
University College London Hospitals 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 |
