Randomised, prospective study of CUSA versus radio frequency ablation technique in liver resections
| ISRCTN | ISRCTN14873873 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN14873873 |
| Protocol serial number | N0205169008 |
| Sponsor | Record Provided by the NHSTCT Register - 2006 Update - Department of Health |
| Funder | Barts and The London NHS Trust (UK), NHS R&D Support Funding |
- 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 of protocol
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
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Study type | Participant information sheet |
| Scientific title | Randomised, prospective study of CUSA versus radio frequency ablation technique in liver resections |
| Study objectives | 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 |
| Health condition(s) or problem(s) studied | Surgery: Liver |
| Intervention | CUSA versus radio frequency ablation technique |
| Intervention type | Procedure/Surgery |
| Primary outcome measure(s) |
Blood loss and blood product requirements. |
| Key secondary outcome measure(s) |
Morbidity, mortality and inflammatory reaction. |
| Completion date | 14/06/2007 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Not Specified |
| Target sample size at registration | 100 |
| Key inclusion criteria | Adult patients referred for liver resection. |
| Key exclusion criteria | 1. Paediatric patients 2. Mentally unable to understand study 3. Unresectable disease 4. Refusal of consent |
| Date of first enrolment | 15/12/2004 |
| Date of final enrolment | 14/06/2007 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Royal London Hospital
London
E1 1BB
United Kingdom
E1 1BB
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 |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Participant information sheet | Participant information sheet | 11/11/2025 | 11/11/2025 | No | Yes |
Editorial Notes
18/01/2016: no publications found on PubMed.
28/02/2018: no publications found,verifying study status with principal investigator.
