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The cardiac and renal protective effects of tolvaptan on peritoneal dialysis patients with volume overload

The cardiac and renal protective effects of tolvaptan on peritoneal dialysis patients with volume overload

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060300
Enrollment
Unknown
Registered
2022-05-26
Start date
2023-05-10
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Capacity overload peritoneal dialysis patients

Interventions

Tolvaptan group:Tolvaptan, 15 mg, QOD, orally every other day (both before and after meals), for a total of 6 months of conventional treatment.
control group:Routine treatment for a total of 6 months.

Sponsors

Department of Nephrology, the second hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Have serious behaviors (self harm, serious repetitive and stereotyped behaviors) or emotional problems (frequent emotional breakdown); 2. Have other disease diagnoses (e.g., visual impairment). 1. Age: 18-70 years; Regularly treat PD for = 1.7 orCcr>=50ml/min; 4. According to bioelectrical impedance measurement, excessive water (OH) >= 1.0L; 5. Have not taken vasopressin V2 receptor antagonists such as lovastatin in the past 3 months; There are no restrictions on natriuretic peptide preparations such as sarcubatrixartan, neobiotin, and traditional diuretics such as furosemide, spironolactone, etc; 6.The patient agreed to the study protocol and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Daily urine volume is greater than 1000ml or less than 100ml; 2. Combined hemodialysis; 3. Hypovolemic hyponatremia, hypernatremia; 4. Due to personal reasons, it is necessary to use it in combination with powerful CYP3A inhibitors (such as ketoconazole, etc.); 5. Complications associated with PD infection and catheter complications; 6. Patients with active infection, malignant tumor, chronic liver disease, and chronic obstructive pulmonary disease; 7. During pregnancy or lactation, women of reproductive age do not agree to use contraception during the trial; 8. Those who plan to undergo kidney transplantation surgery in the past 18 months; 9. Those who have poor compliance and cannot be treated according to the protocol. 10.Patients participating in other clinical trials

Design outcomes

Primary

MeasureTime frame
Capacity load index;

Secondary

MeasureTime frame
Cardiac function index;Renal function index;General status of the patient;Biochemical detection;

Countries

China

Contacts

Public ContactCui Wenpeng

The second hospital of Jilin University

wenpengcui@163.com+86 13504316157

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026