Randomised double blind placebo controlled trial of the efficacy of gabapentin in improving analgesia in patients undergoing hysterectomy receiving patients controlled analgesia
| ISRCTN | ISRCTN54176811 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN54176811 |
| Secondary identifying numbers | N0263156073 |
- Submission date
- 30/09/2005
- Registration date
- 30/09/2005
- Last edited
- 02/11/2016
- 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 of Anaesthesia
The Middlesex Hospital
Mortimer Street
London
W1N 8AA
United Kingdom
| Phone | +44 |
|---|---|
| brigitta.brandner@uclh.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 | Randomised double blind placebo controlled trial of the efficacy of gabapentin in improving analgesia in patients undergoing hysterectomy receiving patients controlled analgesia |
| Study objectives | Does gabapentin reduce morphine use and pain at rest and on movement? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Pain |
| Intervention | 1. Analgesia with gabapentin 2. Standard analgesia |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Gabapentin |
| Primary outcome measure | Morphine use and pain measured by visual analog score |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/10/2003 |
| Completion date | 01/07/2007 |
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 from Anaesthetics |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/10/2003 |
| Date of final enrolment | 01/07/2007 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
The Middlesex Hospital
London
W1N 8AA
United Kingdom
W1N 8AA
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Phone | +44 (0)20 7307 2622 |
|---|---|
| dhmail@doh.gsi.org.uk | |
| Website | http://www.dh.gov.uk/Home/fs/en |
Funders
Funder type
Government
UCL Hospitals NHS Foundation Trust (UK)
No information available
NHS R&D Support Funding
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
02/11/2016: No publications found, verifying study status with principal investigator.
