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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01893710
Other study ID # IPPB Biobank
Secondary ID University of He
Status Recruiting
Phase
First received
Last updated
Start date February 2011
Est. completion date December 2028

Study information

Verified date December 2023
Source Heidelberg University
Contact Claus P Schmitt, Prof
Phone +49 6221 56
Email claus.peter.schmitt@med.uni-heidelberg.de
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Within few years the peritoneal membrane of adult peritoneal dialysis (PD) patients undergoes substantial morphological transformation, including progressive fibrosis, vasculopathy and neoangiogenesis. Ultrafiltration capacity steadily declines and ultimately results in PD failure. In children, peritoneal biopsies demonstrating PD associated alterations have not yet been obtained. They, however, should be particularly informative, since secondary tissue and vascular pathology related to ageing or diabetes is absent. An international, prospective peritoneal membrane biopsy study in children on PD will therefore be performed. Biopsies will be obtained at time of PD catheter insertion, on occasion of intercurrent abdominal surgery (e.g. hernia repair, catheter exchange) and at time of renal transplantation. Quantitative histomorphometry and tissue protein expression analyses will be correlated with time integrated PD treatment modalities and functional characteristics as well as inflammatory and cardiovascular comorbidity surrogate parameter. Blood will be obtained during clinical routine sampling. Biopsies will be obtained during clinically indicated operations, without substantially increasing operation time and associated surgical risks. The detailed histomorphometry of the PD membrane will give additional information, potentially impacting on the individual PD regime. 3/2018: The analyses of the pediatric PD biopsy demonstrated early and major transformation of the peritoneal membrane with neutral pH low GDP fluids, and significant vasculopathy already in children with CKD stage 5, further progressing with PD. The underlying mechanisms are partly understood, only. In view of these major findings and the numerous open questions, collection of biosamples will be continued in children and also in adult PD patients. The following questions will be addressed: Molecular counterparts of peritoneal semi-permeability, solute and water transport (beyond AQP1), pathomechanisms and molecular and functional impact of peritoneal transformation with low and high GDP fluids, and the respective pathomechanisms and molecular and functional impact of vascular disease in CKD and with different PD fluids. The impact of renal transplantation following PD will be assessed in a subgroup of patients with tenckhoff catheter removal several weeks after transplantation and a functioning graft.


Description:

Please see study protocol and http://www.pedpd.org


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date December 2028
Est. primary completion date October 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Day to 90 Years
Eligibility Inclusion Criteria - Age 0 to 90 years - CKD 5D, peritoneal dialysis and - Patients with normal renal function and elective abdominal surgery due to limited abdominal pathology (such as hernia repair, gallstones….) - Patients post PD and post Tx - Oral and written consent - Ability to consent of the adult patient and of the parents and legal guardian of patients not yet of legal age, respectively Exclusion Criteria: - Abdominal adhesions, malformation and inflammation beyond PD induced changes - Patients with disseminated tumour disease - Patients with critical heart failure and other medical conditions, where the additional procedure may confer an increased increase risk - Pregnancy - Preterm babies (below 37 weeks of gestational age) - Serum hemoglobin < 10 g/dl in newborns and < 8 g/dl in children and adults

Study Design


Intervention

Procedure:
biopsy sampling
Two parietal peritoneal samples, each 1 cm² x 0.3 cm in depth and three omental tissue samples, each 1 cm² in size will be obtained. Biopsy sampling will be performed in all groups. This is an observational not an interventional trial.

Locations

Country Name City State
Austria Department of Pediatrics, Medical University Vienna Vienna
Belgium UZ Ghent Ghent
Czechia University Children's Hospital Prague
France Service de Néphrologie Pédiatrique, Hôpital Femme Mere Enfant Lyon
France University Children's Hospital Strasbourg
Germany University Children's Hospital Berlin
Germany University Children's Hospital Cologne
Germany University Children's Hospital Essen
Germany UKE, University Children´s Hospital Hamburg
Germany Department of Medicine I (Nephrology), University of Heidelberg Heidelberg BW
Germany KfH Pediatric Kidney Center, Department of Pediatric Nephrology, University of Marburg Marburg
Hungary University Children's Hospital Budapest
Italy University Children'Hospital Genova
Italy University Children's Hospital Milano
Italy Pediatric Nephrology, Dialysis and Transplant Unit Padova
Lithuania University children's Hospital Vilnius
Malaysia Paediatric CAPD unit, Kuala Lumpur Hospital Kuala Lumpur
Poland Krakow, Jagiellonian University Medical College Krakow
Spain Hospital Universitario Materno-Infantil Vall d' Hebron Barcelona
Sweden Karolinska University Hospital Stockholm
Switzerland Children's Hospital, Inselspital, Bern University Hospital and University of Bern Bern
Turkey University Children's Hospital Adana
Turkey Cerrahpasa School of Medicine Istanbul
United States University of Alabama at Birmingham Birmingham Alabama
United States Children's Mercy Hospital Kansas City Missouri
United States The Children´s Hospital of Philadelphia Narberth Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Heidelberg University

Countries where clinical trial is conducted

United States,  Austria,  Belgium,  Czechia,  France,  Germany,  Hungary,  Italy,  Lithuania,  Malaysia,  Poland,  Spain,  Sweden,  Switzerland,  Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Submesothelial thickness (µm) Digital imaging analysis of submesothelial thickness as a marker of peritoneal fibrosis (distance between mesothelium and adjacent muscle/adipos tissue) 2 years (average PD duration)
Other Submesothelial lymphocyte, macrophage, MMT cell count Quantification of peritoneal leucocyte Infiltration, i.e. number of CD45 positive lymphocytes and CD68 positive macrophages per mm² of submesothelial section area . The number of cells that underwent mesothelial-mesenchymal transition per mm² submesothelial section are quantified by immunohistochemical co-staining of mesothelial and fibroblast marker (cytokeratin and FSP1). 2 years (mean PD duration)
Other Peritoneal VEGF and pSMAD abundance Key cytokines involved in peritoneal membrane transformation will be measured immunohistochemically. These are VEGF and TGF-beta induced p-SMAD (%positive area per section area analysed). 2 years (mean PD duration)
Primary Peritoneal vasculopathy (lumen vessel ratio) Digital quantification of degree of vasculopathy, i.e the lumen vessel ratio. Healthy children have a L/V ratio of about 0.7. lower values represent vasculopathy with lumen narrowing, 0 is complete obliteration of the vessel.
This measurements will be accompanied by molecular analysis of pathomechanisms (including omics Technology)
Two years (Mean PD treatment time)
Secondary Number of vessels per peritoneal membrane area (per mm²) Digital histomorphometry of small vessel density per mm² submesothelial section area analysed. at time of catheter insertion, intercurrent abdominal surgery and at time of renal transplantation
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