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Efficasy and safety of tolvaptan in patients undergoing peritoneal dialysis with heart failure despite the standard treatment with conventional

Efficasy and safety of tolvaptan in patients undergoing peritoneal dialysis with heart failure despite the standard treatment with conventional - Effects of tolvaptan in patients undergoing pertoneal dialysis with heart failure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008712
Enrollment
40
Registered
2012-08-17
Start date
2012-08-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Heart Failure, Chronic Renal Failure

Interventions

Tolvaptane combination group: furosemide at a dose of 120mg daily for 3 days given in combination with tolvaptan 15mg/day Conventional treatment group: furosemide at a dose of 120mg daily for 3 days

Sponsors

Division of Kidney and Hypertension, the Jikei University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)The patients with chronic heart failure 2)The patients undergoing peritoneal dialysis 3)The admitted patients 4)Male and Female 5)The patients over 20 years old in a time of consent 6)The patients with individual or representitive consent

Exclusion criteria

Exclusion criteria: 1)The patients showing allergy to tolvaptan or similar compound (ex. mozavaptan) 2)The patients showing allergy to sulfonamide 3)The anuric patients 4)The patients without a sense of thirst or ability to intake water 5)The patients with hypernatremia 6)The pregnant patients 7)The patients taking tolvaptan at the time of enrolling 8)The patitents in need of emergency medical care for massive heart failure 9)The patients given furosemide over 120mg/day at the time of enrolling 10)The patients with hepatic coma 11)The patients regarded as inappropriate for this clinical study by the principal investigator

Design outcomes

Primary

MeasureTime frame
Change of Body Weight

Secondary

MeasureTime frame
urine volume, urine osmolarity, serum osmolarity, serum electrolyte concentration, hANP, BNP, fluid retention, water intake, NYHA functional classification, serum ADH, creatinine clearance, urine electrolyte concentration, total removed fluid with PD

Countries

Japan

Contacts

Public ContactHiroshi Hayakawa M.D., Ph.D.

The Jikei University School of Medicine Division of Kidney and Hypertension

03-3433-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026