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

Anaesthetics Department
Middlesex Hospital
Mortimer Street
London
W1N 8AA
United Kingdom

Phone +44 (0)20 7636 8333
Email abc@email.com

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Scientific titleA comparison of subcutaneous morphine and diamorphine given via patient-controlled analgesia after hip replacement
Study objectivesIs 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) studiedSigns and Symptoms: Pain
Intervention1. Subcutaneous morphine
2. Diamorphine
Intervention typeDrug
PhaseNot 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 date01/09/2004

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Target sample size at registration40
Key inclusion criteriaNot provided at time of registration
Key exclusion criteriaNot provided at time of registration
Date of first enrolment30/03/1999
Date of final enrolment01/09/2004

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Middlesex Hospital
London
W1N 8AA
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan