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Completed

NCT Number: NCT01741363

Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing

1. The abundant results from this trial will be helpful for assessing the feasibility of increasing stool sampling and shortening screening interval in population setting for lower and upper gastrointestinal tract lesions, their long-term effects, and the respective cost-effectiveness. 2. The study will evaluate the value of population-based screen and treatment for H. pylori infection when the HPSA is combined with the FIT.

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Key information

Age range

50 year–69 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Taiwan University Hospital

Taipei, 10002, Taiwan

About this study

Growing body of evidences have shown that fecal immunochemical test (FIT) outperform guaiac fecal occult blood test (gFOBT) in terms of sensitivity, neoplasm detection rate and public participation. Though direct outcome evidence is still lacking for FIT, it is anticipated to have higher colorectal cancer (CRC) mortality and incidence reduction compared with gFOBT. In Taiwan, nation-wide CRC screening program has been launched since the year of 2004 ,which provides biennial FIT screening for adults aged 50 to 69 years. Currently available data from the Bureau of Health Promotion has shown a significant stage-shift effect, an early indicator of screening effectiveness, by this screening program.

Nevertheless, the aforementioned advantages of FIT, missed neoplasms and interval cancer still exists under the current one-day stool sampling method with biennial screening interval, which might affect the effectiveness of overall screening program. Increase the number of stool samples or shortening of screening interval may be helpful for early detection of clinically significant neoplasms but it remains unclear whether such an approach may lower the screenee compliance or public participation. Moreover, its impact on the demand of confirmatory colonoscopy and cost-effectiveness of the whole screening program is still largely unknown and need to be further investigated.

In this study, we firstly aim to randomly allocate screening attendee to one of the following four arms: one-day sampling with annual screening, one-day sampling with biennial screening, two-day sampling with annual screening, and two-day sampling with biennial screening. Participation rate, positive rates of FIT, detection rate for neoplasms, positive predictive value, and long-term outcome including cancer incidence and mortality will be calculated and compared among four groups.

Secondly, in the Taiwanese population, which is a typical presentation of Asian populations, although the incidence of colorectal cancer is rapidly increasing, Helicobacter pylori-related upper gastrointestinal pathologies remain highly prevalent, which may imply that mass screening solely based on FIT could be insufficient as significant upper GI pathologies can be missed. Since the FIT does not predict upper GI pathologies, the adjunct of an「Helicobacter pylori stool-antigen test (HpSA) 」 may be a potential candidate to realize a pan-detecting assay based on stool samples in a population in which both lower and upper GI lesions are equally prevalent. Therefore, in the present study, we will also evaluate the value of simultaneous FIT and HpSA test in the community-based mass screening. We invited subjects in a randomized study to receive the FIT or the FIT plus HPSA. Those who are tested positive for HPSA will receive upper endoscopic examination and anti-H. pylori treatment. For the short-term indicators, we will evaluate the participation rate and diagnostic yield when the HPSA is added. For the long-term indicators, we will compare the incidence and mortality of gastric cancer as well as complicated peptic ulcers.

To summary, this study includes two randomized trials:

  • To make a comparison between one-day sampling with annual screening, one-day sampling with biennial screening, two-day sampling with annual screening, and two-day sampling with biennial screening using FIT;
  • To make a comparison between FIT plus HpSA and FIT alone for screening.

Finally, the cost-effectiveness analysis will be also conducted using previously established Markov model of CRC natural history and stomach diseases (such as dyspepsia, peptic ulcer disease, and gastric cancer) using the results ascertained from this trial. The primary outcomes were gastric cancer incidence and mortality rates as well as colorectal cancer incidence and mortality rates.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 50 to 69 years average-risk subjects for FIT
  • 50 to 69 years subjects for HpSA

Exclusion criteria

(for the FIT-based RCT):

  • Subjects who are unwilling to participate
  • Subjects ineligible for colonoscopy (for the one-day vs two day FIT screening)

Exclusion criteria

(for the FIT+HPSA vs. FIT-only RCT)

  • Subjects with a history of total gastrectomy
  • Pregnancy
  • Subjects with severe illnesses
  • Subjects with prior participation in the pilot program

Treatment and study plan

FIT(Eiken OC-Sensor) Two-day sampling

Other

Collect two stool samples in two separate days

FIT(Eiken OC-Sensor) One-year interval

Other

Screening with one-year interval

FIT(Eiken OC-Sensor) One-day sampling

Other

One-day sampling

FIT(Eiken OC-Sensor) Two-year interval

Other

Screening with two-year interval

HpSA (Firstep Helicobacter pylori Antigen Rapid Test)

Other

HpSA for detection of upper gastrointestinal diseases; screen and treat for H. pylori infection. Upper endoscopy for H. pylori carriers. HPSA+FIT compared with FIT alone.

FIT only

Other

HPSA+FIT compared with FIT alone.

Primary outcomes

  1. Incidence of Stomach Cancer

    Time frame: 5.5 years

    Number of incident stomach cancer

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

  2. Mortality of Stomach Cancer

    Time frame: 5.5 years

    Number of stomach cancer death

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Secondary outcomes

  1. Mortality of Colorectal Cancer

    Time frame: 5.5 years

    Number of colorectal cancer death

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

  2. Incidence of Colorectal Cancer

    Time frame: 5.5 years

    Number of incident colorectal cancer

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Other outcomes

  1. Helicobacter Pylori Eradication Rate

    Time frame: 5.5 years

    Subjects who received anti-H. pylori treatment.

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

  2. Confirmatory Examination Referral Rate

    Time frame: 5.5 years

    Subjects who received confirmatory examinations (colonoscopy or flexible sigmoidoscopy plus double contrast barium enema for lower gastrointestinal tract disease; esophagogastroduodenoscopy for upper gastrointestinal tract disease) /subjects with positive stool test (FIT or HpSA)

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

  3. Detection of Advanced Adenoma and Cancer

    Time frame: 5.5 years

    Number of Advanced Adenoma and Colorectal Cancer

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

  4. Participation Rate of HpSA + FIT or FIT Only

    Time frame: 5.5 years

    Number of participants from invitation population

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

  5. Detection of Non-advanced Adenoma

    Time frame: 5.5 years

    Number of non-advanced adenoma from study population

    The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020.

    For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Collaborators

  • Ministry of Health and Welfare, Taiwan

Registry information

Official study title

Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing: a Population-based Randomized Study

Important dates

Study start
2014
Primary completion
2020
Study completion
2020
First posted
Dec 4, 2012
Registry last updated
Nov 21, 2024

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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