Ireland
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Latest
Recruiting Observational

Percutaneous Peritoneal Dialysis Catheter Insertion (PREDICT)

NCT06065982 · tracked via the Priya Life Science Belgium tracker
Phase
Observational
Started
2023-06-23
Last updated
2023-10-04

Condition(s) studied

End-stage Kidney Disease

Investigational drug(s) / intervention(s)

Questionnaires

Questionnaires: Health-related quality of life will be measured using the 12-item Short Form (SF-12) and EQ5D-5L questionnaires. The SF-12 is summarized into two component scores, the Physical Component Score (PCS) and Mental Composite Score (MCS).

Study summary

Peritoneal dialysis (PD) is the most frequent modality of home dialysis for patients with kidney failure.

Most PD catheters are placed using a laparoscopic technique. This approach requires the availability of a qualified surgeon, time in the operating theater and general anaesthesia for the patient. Thus, the laparoscopic technique is less suitable for patients with severe heart failure or multimorbidity where general anaesthesia is not possible.

PD catheters can also be inserted using a percutaneous strategy using a modified Seldinger technique. This strategy can be performed bedside under local anaesthesia, by the nephrologist, radiologist, a surgeon, physician assistant or qualified nurse.

The availability of the percutaneous implantation strategy of a PD catheter in a nephrology center may accomodate more patients to receive a PD catheter insertion, including those who have a contraindication to general anaesthesia or need urgent PD.

The PREDICT project aims to increase knowledge and competencies on percutaneous PD catheter insertions by training centers for this technique. By establisching a prospective registry, the outcomes of percutaneously inserted PD catheters, both in experienced and newly trained centers, will be assessed.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \> 18 years * Percutaneous PD catheter insertion between March 1st 2023 and March 1st 2026 Patients can be included 4 weeks before until 12 weeks after PD catheter insertion Exclusion Criteria: * Inability to provide informed consent * Life expectancy \< 3 months

Primary outcome measure(s)

  • Implementation of percutaneus PD catheter insertion technique in dialysis centers — through study completion, 3 years
    The first co-primary outcome measure assesses the implementation of the percutaneous PD catheter insertion technique in additional dialysis centers.
  • Outcomes of percutaneous inserted PD catheters in participating centers — Over 12 months after percutaneous insertion
    The second co-primary outcome measure assesses the outcomes of percutaneous inserted PD catheters in participating centers: functionality of PD catheters, defined as catheters usable for PD, over 12 months after percutaneous insertion, and taking into account competing events.

Trial sites (2)

FacilityCityRegionStatus
Universitair Ziekenhuis Brussel Brussels Belgium Recruiting
UMC Utrecht Utrecht Netherlands Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06065982 on ClinicalTrials.gov ↗ ← All trials in Belgium