Randomised, prospective study of CUSA versus radio frequency ablation technique in liver resections
| ISRCTN | ISRCTN14873873 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN14873873 |
| Secondary identifying numbers | N0205169008 |
- Submission date
- 29/09/2006
- Registration date
- 29/09/2006
- Last edited
- 28/02/2018
- 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
Not provided at time of registration
Contact information
Mr Robert R Hutchins
Scientific
Scientific
Department of Surgery
Royal London Hospital
Whitechapel
London
E1 1BB
United Kingdom
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 the contact details below to request a patient information sheet |
| Scientific title | Randomised, prospective study of CUSA versus radio frequency ablation technique in liver resections |
| Study hypothesis | To determine which of the two methods established for liver resection results in the least blood loss, lowest blood and blood product requirement, lowest morbidity rate and reduced organ failure score as well as systemic inflammatory reaction. |
| Ethics approval(s) | Not provided at time of registration |
| Condition | Surgery: Liver |
| Intervention | CUSA versus radio frequency ablation technique |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Blood loss and blood product requirements. |
| Secondary outcome measures | Morbidity, mortality and inflammatory reaction. |
| Overall study start date | 15/12/2004 |
| Overall study end date | 14/06/2007 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Not Specified |
| Target number of participants | Initially 80. 100 as of July 2009. |
| Participant inclusion criteria | Adult patients referred for liver resection. |
| Participant exclusion criteria | 1. Paediatric patients 2. Mentally unable to understand study 3. Unresectable disease 4. Refusal of consent |
| Recruitment start date | 15/12/2004 |
| Recruitment end date | 14/06/2007 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Royal London Hospital
London
E1 1BB
United Kingdom
E1 1BB
United Kingdom
Sponsor information
Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Government
Government
The Department of Health
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
Hospital/treatment centre
Barts and The London NHS Trust (UK), 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
18/01/2016: no publications found on PubMed.
28/02/2018: no publications found,verifying study status with principal investigator.
