Actively Recruiting

All Genders
ID07155148

Argentine Registry of Crohn's Disease and Ulcerative Colitis

Led by Grupo Argentino de Enfermedad de Crohn y Colitis Ulcerosa · Updated on 2025-09-23

4250

Participants Needed

1

Research Sites

108 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to create a comprehensive registry of patients with Inflammatory Bowel Disease (IBD) in Argentina, including both children and adults. The registry collects detailed demographic, clinical, and diagnostic information from routine medical care to better understand IBD in this population. It also evaluates safety aspects, such as infections, access to healthcare, and treatment effectiveness, including complications like flares, hospitalizations, and surgeries. The registry is observational, involving no experimental treatments or interventions. It is coordinated by multiple committees overseeing administration, scientific initiatives, and methodological support. Physicians across Argentina who manage IBD patients contribute data through a secure web platform. Participation is voluntary for both doctors and patients, with ethical approval and informed consent processes in place to protect patient privacy. Participants contribute data during routine clinical visits, which are uploaded and monitored centrally to ensure quality and completeness. Researchers analyze information on demographics, treatment safety, and clinical outcomes. The registry supports ongoing research projects to address important regional questions on IBD. Participation duration and follow-up depend on routine care, with data collection continuing over time to support epidemiological studies.

CONDITIONS

Brief Title

Argentine Registry of Crohn's Disease and Ulcerative Colitis

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Any patient diagnosed with IBD defined by validated diagnostic criteria
Not Eligible

You will not qualify if you...

  • Suspected IBD diagnosis without confirmation
  • IBD patients with incomplete information about therapy and follow-up

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) to confirm diagnosis and consent

Surveillance

Duration - Ongoing throughout the study period

Participants who undergo routine care for inflammatory bowel disease (IBD) are observed through data collection in the registry to capture demographic, clinical, and safety information.

Visits occur as part of routine care with data collected during regular clinical appointments

Trial Site Locations

Total: 1 location

1

Hospital Privado Universitario de Cordoba

Córdoba, Córdoba Province, Argentina, 5016

Actively Recruiting

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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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Published Research Related To This Trial

Development of the global inflammatory bowel disease visualization of epidemiology studies in the 21st century (GIVES-21).

Joyce W Y Mak, Yang Sun, Julajak Limsrivilai...

https://pubmed.ncbi.nlm.nih.gov/37231405

Real-world clinical characteristics and therapeutic strategies in patients with moderate-to-severe inflammatory bowel disease in Argentina: Data from the RISE-AR study.

Pablo Andres Olivera, Domingo Balderramo, Juan Sebastian Lasa...

https://pubmed.ncbi.nlm.nih.gov/39549817

High ulcerative colitis and Crohn's disease ratio in a population-based registry from Córdoba, Argentina.

Domingo Balderramo, Juan Trakal, Pablo Herrera Najum...

https://pubmed.ncbi.nlm.nih.gov/33531211