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Completed

NCT Number: NCT01739608

Participation and Detection Rate of Screening CT Colonography and Screening Sigmoidoscopy

The objectives of this multicenter, randomized trial is to assess the participation rate achievable through two different screening strategies (Computed Tomographic Colonography-CTC and sigmoidoscopy-FS), to compare detection rate of colorectal cancer (CRC) and advanced adenoma of tests and to evaluate their costs. The role of Computer-aided detection (CAD) for CTC screening will be also assessed. The trial involves 10 Italian centers located in the Piedmont Region and in Verona. Residents aged 58-60 years in those districts are target for recruitment. Exclusion criteria include: previous diagnosis of cancer or adenoma; family history or hereditary syndromes; personal history of inflammatory bowel disease; patients screened by colonoscopy or FOBT within 2 years; severe disease.

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Key information

Age range

58 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

S.C.D.O. Epidemiologia dei Tumori - Azienda Ospedaliera S. Giovanni Battista di Torino

Turin, Piedmont, 10123, Italy

About this study

Design:

  • To compare detection of advanced neoplasia of CT colonography (CTC) to sigmoidoscopy (FS), a total of 20.000 eligible individuals living in the target areas are mailed an invitation letter to participate in the trial. All invitees are asked to call the screening centre in order to receive detailed information about study protocol, the screening examinations and the bowel preparation. Responders who consent to participate in the study are randomly assigned to undergo screening with CTC or FS. All non-responders will be invited to Fecal Occult Blood test (FOBT) according to the current screening procedure. In the CTC arm, positive patients (containing at least one polyp 6 mm or larger) are referred to colonoscopy; negative patients (no polyps >5 mm) are scheduled to be invited to have an FOBT after two years. In the FS arm, positive patients (at least one advanced adenoma found during FS examination) are referred to colonoscopy; negative patients are offered no further follow-up.
  • To compare participation rate to FS and CTC, 1200 individuals living in the target areas and never screened for colorectal cancer, are randomly assigned to receive an invitation for screening with CTC or FS. Individuals of both groups will receive an invitation letter and an information leaflet, containing information about colorectal cancer, importance of screening, and advantages and possible risks of the selected test. Invitation letter for CTC contains a phone number of the screening centre. All invitees are asked to call the screening centre in order to receive information about bowel preparation. All non-responders will receive a remainder by mail after one month. Non-responders to reminder will be invited to FS according with current screening procedure. In the CTC arm, positive patients (containing at least one polyp 6 mm or larger) are referred to colonoscopy; negative patients (no polyps >5 mm) are scheduled to be invited to have an FOBT after two years. In the FS arm, positive patients (at least one advanced adenoma found during FS examination) are referred to colonoscopy; negative patients are offered no further follow-up.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Asymptomatic individuals, at average risk for CRC, 58-60 years old.

Exclusion criteria

  • Personal history of CRC or polyps
  • Family history of CRC or polyps
  • A terminal illness or inflammatory bowel disease
  • Previous five years complete colonoscopy or a FOBT within the previous 2 years
  • Patients who are unable to give informed consent

Treatment and study plan

Invitation to screening

Other

Invitation to screening

Primary outcomes

  1. Detection rate for cancer and advanced adenoma of CT Colonography versus FS in an invitational CRC screening program

    Time frame: three years

    Proportion of subjects detected with CRC or advanced adenomas out of those examined

  2. Participation rate to FS and CT Colonography

    Time frame: one year

    Proportion of subjects attending the proposed examination out of those invited

Secondary outcomes

  1. Number of participants with severe adverse events in both screening groups

    Time frame: three years

    Absolute number of events

  2. Costs of a CRC screening based on CTC

    Time frame: three years

    Unit cost of each procedures for participants

  3. Type of false positive detections of Computer-aided detection for CTC in a CRC screening program

    Time frame: three years

    Characteristics of false positive subjects

Sponsors and collaborators

Lead sponsor

Centro di Riferimento per l'Epidemiologia e la Prev. Oncologica Piemonte

Other

Collaborators

  • Candiolo Cancer Institute - IRCCS
  • Regione Piemonte
  • im3D S.p.A.

Registry information

Official study title

Assessment of the Participation Rate and the Diagnostic Accuracy of a Colorectal Cancer Screening Program: CT Colonography Versus Flexible Sigmoidoscopy. Evaluation of a New Model Based on Telediagnosis

Acronym: Proteus

Important dates

Study start
2013
Primary completion
2014
Study completion
2018
First posted
Dec 3, 2012
Registry last updated
Jan 31, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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