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Evaluating DFPP for Microplastic and PFAS Reduction (DFPP-MNP)

23 juillet 2026 mis à jour par: Proxima Health, Inc.

Removal of Microplastics, Nanoplastics, and PFAS From Human Peripheral Blood Via Double-Filtration Plasmapheresis

This prospective, non-interventional, within-subject paired biomarker study will evaluate whether circulating microplastic and nanoplastic-associated particle concentrations and PFAS concentrations in peripheral blood change after clinically prescribed double-filtration plasmapheresis (DFPP). Twenty adult volunteers already undergoing DFPP independent of research participation will provide paired pre- and post-treatment blood samples. The primary endpoints are within-participant change in microplastic and nanoplastic-associated particle concentration measured by nano-flow cytometry with Nile Red staining, and PFAS concentration measured by LC-MS/MS. An exploratory subset of five participants will undergo Py-GC-MS analysis of paired blood samples and DFPP eluate to evaluate polymer-specific mass changes and the presence of plastic polymers in eluate, and LC-MS/MS to evaluate the presence of PFAS in eluate. DFPP treatment decisions and procedural parameters are determined solely by the treating physician as part of routine care.

Aperçu de l'étude

Description détaillée

Background and Rationale:

Microplastics and nanoplastics (MNPs) have been detected in human blood and every major organ. Increasingly, studies associate MNP exposure with a range of health conditions, including cardiovascular disease, metabolic disease, gastrointestinal disease, neurodegenerative disease, and cancer. There has been very little study of clinical approaches to remove MNPs from the human body. Such efforts have been limited in part by challenges in measuring MNPs in human blood, especially nanoplastics, which are too small to be detected by most equipment.

Double-filtration plasmapheresis (DFPP) is an established treatment for dozens of health conditions mediated by substances circulating in plasma. In DFPP, a first filter separates blood cells from plasma, and a second filter removes molecules from plasma according to the filter characteristics. The filtered plasma and blood cells are then recombined and returned to the patient. In 2025, a study showed that the material removed from plasma by a specialized type of DFPP called Inuspheresis with the CE-marked IN300 device includes microplastic molecules.

Per- and polyfluoroalkyl substances (PFAS) are persistent environmental chemicals that can also be measured in human blood and have been associated with a range of health conditions. This study will additionally evaluate whether circulating PFAS concentrations change after DFPP.

Study Design:

This is a single-group, open-label, prospective, within-subject observational pilot study. Approximately 20 adult participants who have already been independently prescribed DFPP by their treating clinic will be enrolled. Study samples and research data will be anonymized before research analysis.

Procedures:

Each participant provides written informed consent, then undergoes blood sampling shortly before the DFPP treatment session and again within 10 minutes of the end of the treatment session, after approximately 0.75 plasma volumes have been treated. Adverse events and tolerability observations are recorded throughout the treatment encounter. For a randomly selected subset of five participants, additional exploratory analyses will be performed on paired blood samples using pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS), and a sample of DFPP eluate will be collected to assess whether plastic polymers and PFAS are present in the material removed during treatment.

Analytical Methods:

Co-Primary: Nano-flow cytometry with Nile Red staining, which has been shown in multiple studies to provide detection and counting of microplastic and nanoplastic particles down to approximately 50 nanometers in human blood.

Co-primary: Liquid chromatography-tandem mass spectrometry (LC-MS/MS) for measurement of total quantified PFAS concentration in paired pre- and post-treatment blood samples from all participants.

Exploratory: Py-GC-MS for polymer-specific mass quantification in blood and eluate in a five-participant subset. PFAS analytes in eluate will also be evaluated in the same subset.

Statistical Analysis:

The primary analyses will evaluate within-subject change in circulating MNP particle concentration and total quantified PFAS concentration using a paired pre/post design. The primary hypothesis tests will be the Wilcoxon matched-pairs signed-rank test. Effect size will be summarized using the median within-participant percent change and geometric mean post/pre ratio with a 95% confidence interval. Based on an approximate paired-analysis power calculation, a sample size of 20 participants provides approximately 80% power to detect a large within-participant reduction on the order of 50%, assuming a two-sided alpha of 0.05 and variability of paired log post/pre ratios not materially exceeding approximately 1.0. The same paired sample size will be used to characterize the PFAS co-primary endpoint. Because this is an early paired biomarker study with two co-primary endpoints, no formal multiplicity adjustment is planned, and the co-primary p-values will be interpreted descriptively. Exploratory Py-GC-MS analyses in the five-participant subset are not powered for definitive hypothesis testing; results will be summarized using absolute and percent change. Exploratory PFAS eluate results will be summarized descriptively. Quality-control procedures include procedural blank review; values at or below the laboratory limit of quantification will be treated conservatively.

Type d'étude

Observationnel

Inscription (Estimé)

20

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Obergünzburg, Allemagne
        • Ayus Medical Buergenstock - Buergenstock Resort Lake Lucerne
      • Basel, Suisse, 4051
        • Ayus Medical Basel AG

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

Adults aged 18 to 80 who have already been independently prescribed and medically cleared for DFPP by a qualified treating clinic and who are willing and able to provide paired pre- and post-treatment blood samples.

La description

Inclusion Criteria:

  • Age 18 to 80 years
  • Body weight greater than 40 kg (approximately 88 lb)
  • Already independently prescribed DFPP treatment by a qualified treating clinic
  • Able to understand the study and provide voluntary informed consent
  • Willing and able to provide blood samples before and after DFPP treatment
  • Cleared for DFPP by the prescribing clinic
  • Has not had plasmapheresis treatment within the past 7 days

Exclusion Criteria:

  • Not yet prescribed DFPP by a treating clinic
  • Major heart or circulatory problems, such as recent myocardial infarction or hypertensive crisis
  • Serious kidney or liver impairment
  • Blood-clotting disorders or significantly impaired coagulation
  • Active infection, inflammation, or fever
  • Severe frailty or very poor medical condition
  • Anemia with hemoglobin below 8 g/dL
  • Body weight under 40 kg
  • Pregnancy or breastfeeding
  • Determined by the treating clinic to be medically or mentally inappropriate for DFPP

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
Intervention / Traitement
DFPP Treatment Group
Adults aged 18 to 80 who have already been independently prescribed DFPP by their treating clinic, independent of research participation. Each participant undergoes one DFPP treatment session with paired pre- and post-treatment blood sampling. A randomly selected subset of five participants will also provide samples for exploratory Py-GC-MS analysis and eluate collection.
A single clinically prescribed session of double-filtration plasmapheresis using the IN300 Inuspheresis apheresis device. Blood is withdrawn through intravenous access, passed through a primary filter that separates plasma from blood cells, and then through a secondary filter that removes particles according to the filter characteristics. The filtered plasma and blood cells are recombined and returned to the participant. The session treats approximately 0.75 plasma volumes. DFPP is prescribed by and performed at the treating clinic outside the scope of the research study.
Autres noms:
  • Plasmaphérèse
  • Inuspheresis
  • DFPP

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in Circulating Microplastic and Nanoplastic Particle Concentration
Délai: Baseline immediately before DFPP and post-treatment within 10 minutes of the end of the DFPP session, within a single treatment day
Within-subject change in total microplastic and nanoplastic particle concentration in peripheral blood, measured by nano-flow cytometry with Nile Red staining and reported as particles per unit volume, absolute change, percent change, and post/pre ratio. Pre-treatment and post-treatment blood samples are compared within each participant.
Baseline immediately before DFPP and post-treatment within 10 minutes of the end of the DFPP session, within a single treatment day
Change in Circulating PFAS Concentration
Délai: Baseline immediately before DFPP and post-treatment within 10 minutes of the end of the DFPP session, within a single treatment day
Within-subject change in total quantifiable PFAS concentration in peripheral blood, measured by LC-MS/MS and reported as particles per unit volume, absolute change, percent change, and post/pre ratio. Pre-treatment and post-treatment blood samples are compared within each participant.
Baseline immediately before DFPP and post-treatment within 10 minutes of the end of the DFPP session, within a single treatment day

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in Total Plastic Polymer Mass Concentration by Py-GC-MS in a Subset of 5 Participants
Délai: Baseline and post-treatment within a single treatment day; assessed in a randomly selected five-participant subset
Paired pre- and post-treatment blood samples will be analyzed by Py-GC-MS to measure total plastic polymer mass concentration. Results will be summarized by absolute and percent change within participants.
Baseline and post-treatment within a single treatment day; assessed in a randomly selected five-participant subset
Presence of Plastic Polymers in DFPP Eluate
Délai: During a single DFPP treatment session; eluate collected during DFPP
In the same five-participant Py-GC-MS subset, a sample of DFPP eluate will be analyzed by Py-GC-MS to assess whether plastic polymers are detectable in the material removed during treatment.
During a single DFPP treatment session; eluate collected during DFPP
Incidence and Severity of Adverse Events and Tolerability Findings
Délai: During and immediately following the DFPP treatment session
Incidence, nature, and severity of adverse events and tolerability findings recorded during the treatment encounter, including vital-sign monitoring, symptoms, complications, and any medical interventions required.
During and immediately following the DFPP treatment session
Concordance in Direction of Change Between Nano-Flow Cytometry Particle Counts and Py-GC-MS Polymer Mass
Délai: Baseline and post-treatment within a single treatment day; Py-GC-MS assessed in a subset of participants
Exploratory analysis examining whether the change in MNP levels measured by nano-flow cytometry is in the same direction as the change measured by Py-GC-MS. Concordance will be summarized descriptively; no formal hypothesis testing is planned.
Baseline and post-treatment within a single treatment day; Py-GC-MS assessed in a subset of participants
Baseline Correlations of MNP and PFAS Levels With Demographic Characteristics
Délai: Baseline only, before DFPP
Exploratory analysis examining whether pre-treatment MNP levels in peripheral blood are associated with participant demographic characteristics. This outcome does not test treatment efficacy.
Baseline only, before DFPP
Change in Individual PFAS Analyte Concentrations
Délai: Baseline and post-treatment within a single treatment day; post-treatment sample collected within 10 minutes of completion of DFPP.
Paired pre- and post-treatment EDTA whole-blood samples from all participants will be analyzed by LC-MS/MS. Within-participant absolute and percent changes in individual target PFAS analytes will be summarized descriptively. These analyses are exploratory beyond the co-primary total quantified PFAS endpoint.
Baseline and post-treatment within a single treatment day; post-treatment sample collected within 10 minutes of completion of DFPP.
Presence and Quantity of PFAS Analytes in DFPP Eluate
Délai: During a single DFPP treatment session; eluate collected during DFPP.
In the same five-participant exploratory subset used for Py-GC-MS analysis, a sample of DFPP eluate will be analyzed by LC-MS/MS to assess the presence and quantity of PFAS analytes in material removed during treatment. Results will be summarized descriptively and interpreted as supportive or mechanistic evidence rather than as a powered endpoint.
During a single DFPP treatment session; eluate collected during DFPP.
Association Between Baseline MNP and PFAS Levels
Délai: Baseline only, before DFPP.
Exploratory analysis examining whether baseline pre-treatment MNP concentration measured by nano-flow cytometry is associated with baseline total quantified PFAS concentration measured by LC-MS/MS. Associations will be summarized descriptively and may be evaluated using rank-based correlation methods.
Baseline only, before DFPP.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Collaborateurs

Les enquêteurs

  • Directeur d'études: Matthew Amsden, Efforia, Inc
  • Chercheur principal: Jordi Petriz, PhD, Institut de Recerca Germans Trias i Pujol (IGTP)
  • Chercheur principal: Stefan Bornstein, MD, University Hospital Carl Gustav Carus, Technische Universitaet Dresden
  • Directeur d'études: Michael Petegorsky, Proxima Health, Inc.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

12 juin 2026

Achèvement primaire (Estimé)

1 août 2026

Achèvement de l'étude (Estimé)

1 septembre 2026

Dates d'inscription aux études

Première soumission

14 juin 2026

Première soumission répondant aux critères de contrôle qualité

14 juin 2026

Première publication (Réel)

22 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

24 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

23 juillet 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

Individual-level results will be returned directly to participants. Aggregate and de-identified findings will be published or otherwise made publicly available after study completion. No formal plan is currently established to share individual participant data with external researchers for this pilot study.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Oui

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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