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Research on the Mechanism and Clinical Efficacy of Artificial IHDF in Regulating Hypertension during Hemodialysis

Research on the Mechanism and Clinical Efficacy of Artificial IHDF in Regulating Hypertension during Hemodialysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115773
Enrollment
Unknown
Registered
2025-12-31
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Uremic stage of chronic renal failure

Interventions

HD Group:In the first week, HD treatment was received, followed by a two-week elution period (i.e., recovery to conventional HD). In the fourth week, artificial IHDF treatment was received. At the end
IHDF Group:In the first week, artificial IHDF treatment was received, followed by a two-week elution period (i.e., recovery to conventional HD). In the fourth week, HD treatment was received. At the e

Sponsors

Nanchang University First Affiliated Hospital Gaoxin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Have received regular hemodialysis in our hospital for more than 3 months; (2) It conforms to the fourth clinical classification of hemodialysis combined with hypertension in the "Standard Operating Procedures for Blood Purification", namely the RAAS/SNS over-activation type; (3) Voluntarily sign the informed consent form and agree to participate in the research; (4) Age: 18 to 75 years old.

Exclusion criteria

Exclusion criteria: (1) Combined with malignant tumors; (2) Severe heart or lung system diseases have occurred within three months, such as heart failure, malignant arrhythmia, respiratory failure, etc. (3) Those with a history of neurological or mental system diseases; (4) Severe infection; (5) Patients with secondary hypertension other than renal hypertension who meet the fourth clinical classification of hypertension combined with hemodialysis as stipulated in the "Standard Operating Procedures for Blood Purification"; (6) Patients whose antihypertensive regimens were adjusted during the trial.

Design outcomes

Primary

MeasureTime frame
The fluctuation range of systolic blood pressure/diastolic blood pressure;

Secondary

MeasureTime frame
Adverse events;Serious adverse events;SNS, RAAS axis activity, endothelial function, vascular function;Ultrafiltration compliance rate;The usage rate of antihypertensive drugs;The incidence of hypertension during dialysis;

Countries

China

Contacts

Public ContactFeifei Wu

Nanchang University First Affiliated Hospital Gaoxin Hospital

feifeiy2012@163.com+86 791 86319140

Outcome results

None listed

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