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Study identifier: NCT07111260 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy of pHA130 Hemoadsorption for 4 Hours (p4H Study)

Condition: End Stage Renal Disease on Dialysis  ·  Sponsor: Peking University People's Hospital

PhaseNA
Planned participants34
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is an open-label, randomized, crossover study to evaluate the efficacy of extending the duration of hemoadsorption (HA) combined with hemodialysis (HD) from 2 hours to 4 hours for clearing protein-bound uremic toxins, such as Indoxyl Sulfate (IS), in stable maintenance hemodialysis patients. Patients will be randomized to receive either 2-hour HA or 4-hour HA once a week for 8 weeks, then cross over to the other treatment for another 8 weeks after a 2-week washout period. The primary endpoint is the reduction rate of IS.

This description comes directly from the study's public registry record.

Talk to the study team

Liangying Gan  ·  010-88324516  ·  ganl@bjmu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Peking University People's HospitalBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07111260