Unique ID issued by UMIN | UMIN000014134 |
---|---|
Receipt number | R000015841 |
Scientific Title | The effect of tolvaptan on renal function during intensive treatment in patients with congestive heart failure |
Date of disclosure of the study information | 2014/05/31 |
Last modified on | 2014/11/04 21:20:05 |
The effect of tolvaptan on renal function during intensive treatment in patients with congestive heart failure
Renoprotective effect of tolvaptan in acute phase of patients with congestive heart failure
The effect of tolvaptan on renal function during intensive treatment in patients with congestive heart failure
Renoprotective effect of tolvaptan in acute phase of patients with congestive heart failure
Japan |
congestive heart failure
Cardiology | Nephrology |
Others
NO
To compare the effect on renal function, hemodynamics and neurohumoral factors in acute phase of HF patients between tolvaptan and furosemide.
Safety,Efficacy
renal function
1. daily urine volume, fluid balance
2. plasma renin activity, plasma aldosterone concentration, catecholamines, BNP
3. systemic blood pressure
4. electrolytes
5. cardio-thoracic ratio
6. durations of NIPPV use, CCU and total hospitalization
7. in-hospital and long-term mortality
Interventional
Parallel
Randomized
Individual
Open -no one is blinded
Active
NO
NO
Institution is considered as a block.
NO
Numbered container method
2
Treatment
Medicine |
(Standard treatment group)
Daily 40 mg of intravenous furosemide (20 mg x 2), in addition to intravenous 0.025 gamma of carperitide and 200 mg of canrenoate potassium for 5 days. Renal functions and neurohumoral factors were evaluated on day 6 after the admission.
(Tolvaptan treatment group)
Daily 7.5 mg of oral Tolvaptan administration (7.5 mg x 1), in addition to intravenous 0.025 gamma of carperitide and 200 mg of canrenoate potassium for 5 days. Renal functions and neurohumoral factors were evaluated on day 6 after the admission.
30 | years-old | < |
Not applicable |
Male and Female
Patient urgently hospitalized due to acute heart failure syndrome, or worsened chronic heart failure, with informed consent.
(i) Patient with malignant neoplasm who is expected that life expectancy is within 6 months
(ii) Maintenance dialysis patient
(iii) Patient with shock or pre shock vital signs on admission
(iv) Patient younger than 30 years old
(v) Inadequate patient judged by principal investigator
80
1st name | |
Middle name | |
Last name | Kentaro Jujo |
Nishiarai Heart Center Hospital
Department of Cardiology
1-12-8, Nishiarai Honcho, Adachi-ku, Tokyo, Japan
+81358380730
juken1123@hotmail.co.jp
1st name | |
Middle name | |
Last name | Kentaro Jujo |
Nishiarai Heart Center Hospital
Department of Cardiology
1-12-8, Nishiarai Honcho, Adachi-ku, Tokyo, Japan
+81358380730
juken1123@hotmail.co.jp
Nishiarai Heart Center Hospital
Nishiarai Heart Center Hospital
Other
NO
西新井ハートセンター病院
2014 | Year | 05 | Month | 31 | Day |
Unpublished
Completed
2012 | Year | 12 | Month | 01 | Day |
2013 | Year | 01 | Month | 01 | Day |
2014 | Year | 05 | Month | 31 | Day |
2014 | Year | 11 | Month | 04 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015841