Does furosemide improve renal function in patients stopping renal replacement therapy?
| ISRCTN | ISRCTN86755640 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN86755640 |
| Protocol serial number | N0060110642 |
| Sponsor | Department of Health |
| Funder | Chelsea and Westminster Healthcare NHS Trust (UK) |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 02/02/2017
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Urological and Genital Diseases
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 Neil Soni
Scientific
Scientific
Magill Dept of Anaesthetics, 3rd Floor, D Lift
Chelsea & Westminster Hospital
369 Fulham Road
London
SW10 9NH
United Kingdom
| Phone | +44 (0)20 8237 2763 |
|---|---|
| n.soni@imperial.ac.uk |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial parallel design |
| Secondary study design | Randomised controlled trial |
| Study type | Participant information sheet |
| Scientific title | Does furosemide improve renal function in patients stopping renal replacement therapy? |
| Study objectives | Does furosemide improve renal function in patients stopping renal replacement therapy? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Urological and Genital Diseases: Renal function |
| Intervention | Furosemide vs no furosemide |
| Intervention type | Drug |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Furosemide |
| Primary outcome measure(s) |
Change in creatinine clearance after 24 hours of receiving, or not, furosemide infusion |
| Key secondary outcome measure(s) |
Other outcome measures include rate of resumption of renal replacement therapy, peak creatinine, requirement for mineral replacement |
| Completion date | 31/07/2007 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 50 |
| Key inclusion criteria | 50 patients. 1 per week. |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 11/02/2002 |
| Date of final enrolment | 31/07/2007 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Chelsea & Westminster Hospital
London
SW10 9NH
United Kingdom
SW10 9NH
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
02/02/2017: No publications found, verifying study status with principal investigator.
