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CompletedNCT07348913Updated Jan 16, 2026

Impact of Regular Low-Frequency Hemoperfusion on Medium- to Long-Term Prognosis in Maintenance Dialysis Patients

An observational study in Regular Low-Frequency Hemoperfusion, Medium- to Long-Term Prognosis and Maintenance Dialysis Patients, sponsored by Yunfeng Xia. Completed at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-16.

Sponsored by Yunfeng Xia · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
879
Ages
18 Years and older
Sex
All
01

Study summary

Objective: To investigate the effect of regular low-frequency hemoperfusion on all-cause mortality and cardiovascular/cerebrovascular mortality risk in maintenance hemodialysis (MHD) patients.

Methods: Data from MHD patients over the past 10 years at our blood purification center were retrospectively collected. Patients were divided into a hemoperfusion group (receiving regular low-frequency hemoperfusion once monthly) and a non-hemoperfusion group. Propensity score matching (PSM) was used to balance baseline characteristics. Differences in cumulative all-cause and cardiovascular/cerebrovascular mortality between the two groups before and after matching were compared. A competing risk model was employed to analyze mortality risk.

Read the detailed description

Clinical and laboratory data were collected for all enrolled patients. These included age, sex, underlying medical conditions, dialysis vintage, blood pressure, serum albumin, hemoglobin, platelet count, C-reactive protein (CRP), serum calcium, serum phosphorus, intact parathyroid hormone (iPTH), total cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), triglycerides, and serum β2-microglobulin. Time-averaged mean values were calculated for blood pressure and laboratory parameters across the entire follow-up period. Data on cardiovascular/cerebrovascular death and all-cause mortality over the past ten years were also compiled.

Given the considerably larger size of the Hemoperfusion Group compared with the Non-Hemoperfusion Group, propensity score matching (PSM) was performed by specialized statisticians during data processing to balance baseline characteristics between the two groups. This approach enabled a systematic assessment of the effect of regular low-frequency hemoperfusion on cardiovascular/cerebrovascular and all-cause mortality in MHD patients.

02

Conditions studied

  • Regular Low-Frequency Hemoperfusion
  • Medium- to Long-Term Prognosis
  • Maintenance Dialysis Patients
  • Retrospective Study

Keywords

  • Hemoperfusion
  • Maintenance Dialysis
  • Propensity Score Matching
  • Survival Analysis
  • Competing Risk
  • Cardiovascular/Cerebrovascular Death
03

In context

Lead sponsor

Yunfeng Xia is the lead sponsor of 4 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients who received MHD treatment at the Hemodialysis Center of the First Affiliated Hospital of Chongqing Medical University from January 2015 to December 31, 2024. Included patients were aged ≥18 years, received dialysis three times a week (each session lasting 3-4 hours), had basically complete clinical and laboratory records, and were followed up at our center for at least 6 months.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Included patients were aged ≥18 years
  • Undergo dialysis treatment three times a week (each session lasting 3-4 hours)
  • Having basically complete clinical and laboratory records, and having received at least 6 months of follow-up at this center

Exclusion criteria

Exclusion Criteria:

  • Under 18 years old
  • Does not receive dialysis three times a week (each session lasts 3-4 hours)
  • Does not have basic complete clinical and laboratory records, and has not been followed up at this center for at least 6 months
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
879 participants (actual)
Patient registry
No

Groups and cohorts

  • hemoperfusion group

    receive regular low-frequency hemoperfusion once monthly

  • non-hemoperfusion group

    not receive regular low-frequency hemoperfusion once monthly

06

What researchers measure

Primary outcomes

  1. Cardiovascular/Cerebrovascular Death

    Time frame: 1, 3, 5, and 10 years

  2. all-cause mortality

    Time frame: 1, 3, 5, and 10 years

07

Study locations

1 site
  • First Affiliated Hospital of Chongqing Medical University
    Chongqing, Chongqing Municipality 400016, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07348913
Lead sponsor
Yunfeng Xia
Responsible party
Yunfeng Xia (Chief Physician of Nephrology、Clinical Professor, First Affiliated Hospital of Chongqing Medical University) — Sponsor-investigator
First posted
Jan 16, 2026
Start date
Jan 1, 2015
Primary completion
Dec 31, 2024
Completion
Dec 31, 2024
Last update
Jan 16, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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