A comparison of subcutaneous morphine and diamorphine given via patient-controlled analgesia after hip replacement
| ISRCTN | ISRCTN49142784 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN49142784 |
| Protocol serial number | N0263048370 |
| Sponsor | Department of Health (UK) |
| Funder | University College London Hospitals NHS Trust (UK) |
- 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
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| 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 |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Morphine and diamorphine |
| Primary outcome measure(s) |
Subjective visual analogue scores for pain, nausea, sedation and euphoria. |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/09/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 40 |
| 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
- United Kingdom
- England
Study participating centre
Middlesex Hospital
London
W1N 8AA
United Kingdom
W1N 8AA
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 |