Actively Recruiting

Age: 18Years +
All Genders
ID06775951

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Colonoscopies performed in emergency or urgent settings

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Single timepoint

Participants undergo colonoscopy as part of their routine diagnostic examination to evaluate gastrointestinal conditions.

1 visit (in-person)

Long-term Monitoring

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

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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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