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The Factors Affecting IPP in Peritoneal Dialysis Patients with Polycystic Kidney Disease

P

Peking University

Status

Invitation-only

Conditions

Peritoneal Dialysis
Polycystic Kidney Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT06841224
IPP in ADPKD

Details and patient eligibility

About

Background: Polycystic kidney disease (PKD) is the most common hereditary kidney disease. Peritoneal dialysis (PD) in such patients is restricted because the significantly enlarged kidneys and liver may lead to the increase of intraperitoneal pressure (IPP). Increased IPP points to higher risk of abdominal wall complications and limited infusion volume that cause insufficient dialysis adequacy. Therefore, monitoring IPP is especially important in patients with polycystic kidney disease. However, the standard measurement of IPP is limited due to its cumbersome procedures, the application value of equation for estimating IPP among general peritoneal dialysis patients is not clear in the PKD population and the variables influence the IPP is yet to be explored..

Objective: The main purpose of our study was to validate the existing IPP equations in the PKD patients. Further, more relevant variables were included to optimize the IPP equation. Monitoring IPP can guide the formulation of peritoneal dialysis prescription for ADPKD patients, reduce the occurrence of abdominal wall complications, and the clinical utility and efficiency of PD was expanded.

Methods: A multi-center cross-sectional study. The IPPs were measured using the Durand method, with whole-body and abdominal anthropometry indices, the volume of abdominal cavity, the total kidney volume and liver volume were collected. New equation for estimate IPP in PKD patients were generated by stepwise linear regression modeling. The eIPP were calculated using two developed equations previously. Then The bias, accuracy and precision of eIPP derived from new equation were compared with actual IPP by Durand method respectively.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Aged 18-80 years;
  2. A confirmed diagnosis of polycystic kidney disease, with a history of peritoneal dialysis catheter placement and regular peritoneal dialysis;
  3. Able to tolerate the infusion of more than 1500 mL of dialysis fluid.

Exclusion criteria

  1. Acute complications such as peritonitis or cardiovascular and cerebrovascular events within the past month;
  2. History of abdominal surgery or trauma within the past month;
  3. History of kidney cyst rupture, infection, or bleeding within the past month;
  4. History of abdominal or pelvic organ tumors;
  5. History of abdominal pressure-related complications, such as hernias, leaks, or chest-abdominal fistulas;
  6. Unable to attend follow-up visits during the study period;
  7. Refusal to participate in the study. -

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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