Actively Recruiting
Appropriateness of Colonoscopy Indication: an Evaluation of the Clinical and Economic Impact. Multicenter Prospective Observational Study.
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-15
1410
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the appropriateness of colonoscopy prescriptions and their impact on diagnostic performance. The study aims to develop and validate a predictive model to identify patients most likely to have significant lesions, helping reduce costs and waiting times. Colonoscopy is a common procedure, but it can be overused, leading to unnecessary risks and resource waste. The study follows recent prescribing criteria by EPAGE and ASGE to improve colonoscopy use in healthcare systems. This observational study collects data from patients undergoing colonoscopy as part of their regular medical care. Researchers will analyze this information to assess how well the predictive model identifies colonoscopies that find important diagnostic results. The study focuses on patients already scheduled for colonoscopy and involves recording details during their examinations. Participants will be followed for approximately five months to count the number of colonoscopies performed and evaluate their diagnostic findings. Data collection includes patient information during outpatient or inpatient colonoscopy procedures. The study aims to improve colonoscopy use by measuring the frequency and diagnostic value of these examinations, without altering normal care pathways or treatment plans.
CONDITIONS
Brief Title
Appropriateness of Colonoscopy Indication: an Evaluation of the Clinical and Economic Impact.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Patients undergoing outpatient and inpatient colonoscopy for any pathology as part of normal care
- Informed consent obtained
You will not qualify if you...
- Colonoscopies performed in emergency or urgent settings
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single timepoint
Participants undergo colonoscopy as part of their routine diagnostic examination to evaluate gastrointestinal conditions.
1 visit (in-person)
Duration - Approximately 5 months
Participants who undergo routine care are observed to assess outcomes related to colonoscopy indications and diagnostic performance over time.
Trial Site Locations
Total: 2 locations
1
IRCCS Azienda Ospedaliero - Universitaria di Bologna
Bologna, Italy, 40138
Actively Recruiting
2
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Italy, 40138
Actively Recruiting
Research Team
L
Lorenzo Fuccio, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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