Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Retrospective Observational Multicenter Study on the Treatment Patterns, Extra-Intestinal Manifestations, Resource Utilisation, and Outcomes of Patients With Inflammatory Bowel Disease in Dutch Hospitals

26 giugno 2026 aggiornato da: LOGEX

Treatment Patterns, Extra-Intestinal Manifestations, Resource Utilisation, and Outcomes of Patients With Inflammatory Bowel Disease in Dutch Hospitals

This multicenter retrospective real-world data study will evaluate the treatment pathways and disease burden of adult patients with Crohn's disease (CD) and ulcerative colitis (UC) treated in 5-10 Dutch hospitals between 2018 and 2026.

The study will assess:

  • Treatment sequences, switching patterns, and treatment duration
  • Prevalence and incidence of extra-intestinal manifestations (EIMs)
  • Healthcare resource utilization (hospitalizations, outpatient visits, endoscopies, surgery, and length of stay)
  • Direct healthcare costs
  • Availability of disease activity biomarkers

Using linked administrative, prescription, procedure, and laboratory data, outcomes will be analyzed by age, line of therapy, and clinical characteristics. Special focus will be placed on the impact of EIMs on treatment patterns, healthcare utilization, and costs.

The findings will provide real-world evidence on IBD management in the Netherlands and support clinical decision-making, healthcare planning, and future research on treatment optimization and coexisting immune-mediated conditions.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Inflammatory bowel disease (IBD), comprising Crohn's disease (CD) and ulcerative colitis (UC), is a chronic, relapsing inflammatory disorder of the gastrointestinal tract with an increasing global burden. Patients frequently require lifelong management and may experience substantial healthcare resource utilization (HCRU) throughout the course of their disease. Beyond intestinal symptoms, many patients develop extra-intestinal manifestations (EIMs), including rheumatological, dermatological, ophthalmological, and pulmonary conditions, which further increase disease complexity and healthcare burden.

Over the past decade, therapeutic options for IBD have expanded considerably. In addition to conventional treatments such as corticosteroids, thiopurines, methotrexate, and aminosalicylates, multiple classes of advanced systemic therapies (ASTs) are now available, including anti-TNF agents, anti-integrin therapies, anti-IL-12/23 therapies, JAK inhibitors, and S1P receptor modulators. Despite these advances, long-term remission remains challenging for many patients, and there is limited real-world evidence describing how therapies are used in routine Dutch clinical practice, including treatment sequencing, treatment duration, healthcare resource utilization, and outcomes associated with EIMs.

This study aims to address these evidence gaps by generating real-world insights into treatment patterns, EIM burden, healthcare utilization, and costs among patients with CD and UC treated in Dutch hospitals. The findings are intended to support clinical decision-making, healthcare planning, and future research on IBD management in the Netherlands.

Study Design Retrospective, observational, multicenter real-world data cohort study using routinely collected healthcare data from 5 to 10 participating Dutch hospitals. The observational period runs from 1 January 2018 through 31 July 2026 and is fully closed prior to any data extraction. Data are extracted and pseudonymized within participating hospitals before transfer for analysis. No patient contact occurs and no additional data are collected.

Data sources include administrative and claims data, diagnosis registrations, prescription data, electronic prescribing system (EVS) data, laboratory databases, surgical and endoscopy activity data, and intramural medication records. Laboratory data may include fecal calprotectin (fCal), C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), serum albumin, and therapeutic drug monitoring results.

Study Population Adult patients (≥18 years) receiving secondary hospital care with a diagnosis of Crohn's disease or ulcerative colitis, identified between January 2018 and July 2026. The index date is defined as the first confirmed CD or UC diagnosis, requiring at least one healthcare encounter for CD or UC and at least one prescription or dispensing record for an IBD-related medication. Patients who have objected to the use of their data for scientific research are excluded.

Main Research Question Among adult patients with Crohn's disease and ulcerative colitis treated in Dutch hospitals, what are the real-world treatment sequences, treatment duration, healthcare resource utilization, prevalence of extra-intestinal manifestations, and direct healthcare costs over time, and how do these vary according to age, line of therapy, and clinical characteristics?

Study Hypotheses Time-to-discontinuation differs between anti-TNF therapies and other advanced systemic therapy classes used as first-line treatment in patients with CD and UC.

Patients with one or more extra-intestinal manifestations have higher healthcare resource utilization than patients without extra-intestinal manifestations.

Availability and use of objective disease activity markers (fCal, CRP, ESR, and albumin) vary substantially between participating hospitals.

Objectives Primary Objective To describe real-world treatment sequences, treatment duration, healthcare resource utilization, prevalence of extra-intestinal manifestations, and direct healthcare costs among patients with CD and UC, stratified by age, line of therapy, and clinical characteristics.

Secondary Objectives To describe demographic and clinical characteristics of patients with CD and UC.

To quantify the prevalence and incidence of extra-intestinal manifestations. To characterize treatment pathways, treatment switching patterns, and healthcare resource utilization among patients with and without extra-intestinal manifestations.

To explore longitudinal changes in treatment patterns reflecting evolving therapeutic options.

Exploratory Objectives To assess the availability, completeness, and recording frequency of objective disease activity measures, including fecal calprotectin, CRP, ESR, and serum albumin.

To describe advanced therapy dosing patterns and surgical care pathways, including time from first surgery-related outpatient visit to surgery.

Statistical Analysis Analyses will be primarily descriptive. Patient characteristics, treatment pathways, treatment duration, prevalence and incidence of extra-intestinal manifestations, healthcare resource utilization, and costs will be summarized using appropriate descriptive statistics. Treatment duration and time-to-treatment discontinuation will be evaluated using Kaplan-Meier analyses. Treatment sequences will be visualized using Sankey diagrams where appropriate. Comparisons of healthcare utilization and costs between patients with and without extra-intestinal manifestations will be performed using matched descriptive cohorts. Analyses will be conducted using R and reported only for groups containing at least five patients to ensure privacy protection.

Ethical and Legal Framework The study uses retrospective pseudonymized patient data obtained from participating hospitals. Processing is conducted in accordance with the GDPR, including Article 9(2)(j) for scientific research purposes, Article 89(1) regarding appropriate safeguards, and Article 7:458 BW. The coding key remains exclusively under the control of the participating hospitals and is never accessible to LOGEX, investigators, or sponsors. Obtaining individual informed consent is considered impracticable due to the retrospective nature of the study and the large patient population. Patients retain the right to object to the use of their data through their treating hospital. Results will be presented exclusively in aggregated form with a minimum group size of five patients.

Dissemination Publication of study findings in peer-reviewed journals is the primary dissemination objective. Results will also be presented at scientific conferences and reported transparently regardless of the direction or magnitude of the findings. Publications will follow ICMJE authorship criteria and scientific independence will be safeguarded throughout the publication process.

Tipo di studio

Osservativo

Iscrizione (Stimato)

3500

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

secondary and tertiary care, outpatient clinics

Descrizione

Inclusion Criteria:

  • Adult patients (≥18 years of age) who required secondary (hospital) care after January 2018 with a confirmed diagnosis of CD or UC, defined by at least one ICD-10 diagnosis code for CD or UC (K50, K51, K52).

Index date confirmation: the index date is defined as the first date of confirmed CD or UC diagnosis, requiring at least one healthcare encounter for CD or UC AND at least one prescription or dispensing record for any CD or UC-related medication within the observational period.

Exclusion Criteria:

  • Patients who have formally objected to the use of their hospital data for scientific research purposes. Objections are recorded by the treating hospital in the DBC administrative system and automatically transferred to the research dataset, ensuring automatic exclusion from all analyses.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Treatment sequences and duration of conventional and advanced systemic therapies in CD and UC patients
Lasso di tempo: April 2018 - July 2026
April 2018 - July 2026

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Prevalence and incidence of extra-intestinal manifestations (EIMs) per patient per year
Lasso di tempo: April 2018 - July 2026
April 2018 - July 2026
Direct healthcare costs per patient per month
Lasso di tempo: April 2018 - July 2026
April 2018 - July 2026

Altre misure di risultato

Misura del risultato
Lasso di tempo
Availability and completeness of objective disease activity markers (fCal, CRP, ESR, serum albumin)
Lasso di tempo: April 2018 - July 2026
April 2018 - July 2026

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 agosto 2026

Completamento primario (Stimato)

31 marzo 2027

Completamento dello studio (Stimato)

30 giugno 2027

Date di iscrizione allo studio

Primo inviato

26 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

26 giugno 2026

Primo Inserito (Effettivo)

2 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

2 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

26 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • W26.029

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .