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NCT Number: NCT06587997

Changes in Renal Perfusion During Hemodialysis in Patients with End-stage Renal Disease

Residual renal function (RRF) characteristically declines after patients with end-stage renal disease (ESRD) initiate dialysis. Although RRF preservation correlates with improved patient's quality of life and survival prospects, poor understanding of the pathophysiology underlying RRF decline limits protection strategies.

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Key information

About this study

Hemodialysis (HD) is the primary renal replacement therapy for patients with end-stage renal disease. However, residual renal function (RRF) characteristically declines after these individuals start dialysis. This loss of RRF not only impacts the adequacy of dialysis and control of complications but also affects the patient's quality of life and survival prospects. Due to a lack of clear understanding regarding the pathophysiology underlying this decline in RRF, no effective strategies exist for its preservation at present. The objective of this study is to explore the changes in renal perfusion during hemodialysis in patients with end-stage renal disease, and provide a new idea for protection of RRF. This study was an observational study, and no interventions were performed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years;
  • Clinical diagnosis of end-stage renal disease requiring long-term hemodialysis treatment, with dialysis duration ≤ 3 months;
  • Urine output > 500ml/day or GFR > 3ml/min/1.72m2;
  • Signed and dated informed consented is obtained.

Exclusion criteria

  • Presence of vascular access dysfunction (blood flow rate < 180ml/min);
  • Severe heart failure;
  • Active infection;
  • Infectious disease;
  • Patients with severe anemia;
  • Patients with polycystic kidney disease;
  • Expected dialysis duration < 6 months;
  • Pregnancy or lactation women;
  • Patients who are participating in other clinical studies, or who have participated in other clinical studies within 3 months prior to enrollment;
  • Unwillingness to be followed up or poor adherence to treatment;
  • Other circumstances that the investigator considers unsuitable for enrolment.

Treatment and study plan

Primary outcomes

  1. renal perfusion

    Time frame: one day

    Changes in renal perfusion during hemodialysis in patients with end-stage renal disease

Secondary outcomes

  1. diastolic blood pressure

    Time frame: one day

    diastolic blood pressure during hemodialysis in patients with end-stage renal disease

  2. systolic blood pressure

    Time frame: one day

    systolic blood pressure during hemodialysis in patients with end-stage renal disease

  3. urine volume

    Time frame: 10 months

    Urine volume within 10 months of starting dialysis

Study contacts

Contact information is provided by the study sponsor or research team.

Dayang Xie

CONTACT

[email protected]

13718941415

Sponsors and collaborators

Lead sponsor

Yuanjun Yang

Other

Registry information

Official study title

Changes in Renal Perfusion During Hemodialysis in Patients with End-stage Renal Disease: a Prospective Observational Study

Acronym: HD-RPC

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Sep 19, 2024
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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