Actively Recruiting

Age: 18Years +
All Genders
NCT07339709

Intraperitoneal Pressure Measurements Survey in Pediatric Centers

Led by University Hospital, Strasbourg, France · Updated on 2026-01-14

100

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Intraperitoneal pressure (IPP) is an objective measurement used to assess tolerance to fluid volume. IPP has been shown to be strongly correlated with intraperitoneal dialysate volume as well as anthropometric parameters. In observational studies conducted in adults, an IPP greater than 13-14 cmH2O was associated with an increased risk of peritonitis, initiation of hemodialysis, or death. Measuring IPP is therefore a tool to optimize dialysis prescriptions. However, this measurement is not well standardized, and there is limited scientific evidence regarding its impact on patient management. Measuring IPP is a tool to optimize dialysis prescriptions. However, this measurement is not well standardized, and there is limited scientific evidence regarding its impact on patient management. Some centers do not perform any measurements, others perform them monthly, and some only during peritoneal equilibration tests. The hypothesis of this research is to highlight current practices and experiences in measuring intraperitoneal pressures in children undergoing peritoneal dialysis in different European dialysis centers, in order to improve practices regarding PIP prescription.

CONDITIONS

Official Title

Intraperitoneal Pressure Measurements Survey in Pediatric Centers

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthcare professional working in a European dialysis center
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Service de pédiatrie 1 - CHU de Strasbourg - France

Strasbourg, France, 67091

Actively Recruiting

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Research Team

A

Ariane ZALOSZYC, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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