Water warming garment versus forced air warming system in prevention of intraoperative hypothermia during liver transplantation: a randomised controlled trial
| ISRCTN | ISRCTN32154832 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN32154832 |
| Secondary identifying numbers | N/A |
- Submission date
- 29/08/2002
- Registration date
- 29/08/2002
- Last edited
- 05/09/2007
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Digestive System
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English Summary
Not provided at time of registration
Contact information
Dr Piotr K I Janick
Scientific
Scientific
Department of Anesthesiology
Vanderbilt University Medical Center
504 Oxford House
1313 21st Ave S
Nashville
TN 37232-4125
United States of America
| Phone | +1 615 322 3524 |
|---|---|
| Piotr.janicki@mcmail.vanderbilt.edu |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Scientific title | |
| Study hypothesis | Not provided at time of registration |
| Ethics approval(s) | The institutional review board at Vanderbilt University approved the study protocol. |
| Condition | Liver disease |
| Intervention | The intraoperative use of either forced-air warmer or water warming garment for maintenance of patient temperature during surgery |
| Intervention type | Other |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/01/2001 |
| Overall study end date | 01/01/2002 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 24 |
| Participant inclusion criteria | Patients with liver disease undergoing liver transplantation or liver resection under general anesthesia |
| Participant exclusion criteria | Not provided at time of registration |
| Recruitment start date | 01/01/2001 |
| Recruitment end date | 01/01/2002 |
Locations
Countries of recruitment
- United States of America
Study participating centre
Department of Anesthesiology
Nashville
TN 37232-4125
United States of America
TN 37232-4125
United States of America
Sponsor information
Vanderbilt University Medical Center (USA)
Hospital/treatment centre
Hospital/treatment centre
Department of Anesthesiology
504 Oxford House
1313 21st Ave S
Nashville
TN 37232-4125
United States of America
"ROR" |
https://ror.org/05dq2gs74 |
|---|
Funders
Funder type
Hospital/treatment centre
Vanderbilt University Medical Center (USA) - Department of Anesthesiology
No information available
MTRE Advanced Technologies Ltd (Israel)
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 |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | Results | 19/11/2002 | Yes | No |
