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Uptake to Colorectal Cancer Screening in Familial-risk Population

H

Hospital Universitario de Canarias

Status

Completed

Conditions

Screening Uptake of Colonoscopy and FIT
Colorectal Cancer

Treatments

Procedure: annual FIT and colonoscopy in case of a positive test
Procedure: colonoscopy with sedation

Study type

Interventional

Funder types

Other

Identifiers

NCT02567045
Colorectal cancer screening

Details and patient eligibility

About

This is a multicenter, controlled, randomized phase III study to compare participation rate with two screening rounds of fecal occult blood test (FIT) versus one-time screening colonoscopy in first degree relatives (FDR) of patients diagnosed of colorectal cancer (CRC).

The hypothesis of the study is that annual FIT uptake and colonoscopy when a positive test is higher than that of straightforward colonoscopy. Assuming an uptake of 0.50 for colonoscopy and 0.60 for FIT, a Type I error (alpha) of 5% and a power of 90%, 538 FDRs will be necessary to include in each group.

Full description

This is a multicenter, controlled, randomized phase III study to compare participation rate with two screening rounds of FIT versus one-time screening colonoscopy in FDR of patients diagnosed of CRC.

The recruitment process will be programmed through the index case, that will be interviewed to obtain their CRC family history. FDR will be contacted in order to make an appointment in the High-risk CRC Clinic of the participant centers. Randomization will be performed before signing the informed consent to avoid selection bias. A researcher will be responsible to provide detailed information about the study and getting the informed consent. In case of willingness to participate in the study, the FDR will be randomized to one of the following arms: A) One-time colonoscopy; B) annual FIT for two screening rounds and a colonoscopy in case of a positive FIT (cut-off = 10 μg Hemoglobin/g feces). Screening uptake will be defined as the percentage of FDR who participate at least in one of the two FIT screening round in the FIT group or who undergo colonoscopy in the other group. Screening uptake will be calculated under the assumption of intention to screen analysis.

The hypothesis of the study is that annual FIT uptake and colonoscopy when a positive test is higher than that of straightforward colonoscopy. Assuming an uptake of 0.50 for colonoscopy and 0.60 for FIT, a Type I error (alpha) of 5% and a power of 90%, 538 FDRs will be necessary to include in each group.

Enrollment

260 patients

Sex

All

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. FDR with a case index meeting the following conditions: at least one case index < 60 years at diagnosis of the CCR;
  2. having ≥ 2 FDRs with CRC regardless the age of the case index at diagnosis;
  3. having a sibling with CRC;
  4. age <75 years.

Exclusion criteria

  1. past CRC screening;
  2. inflammatory bowel disease or past history of colorectal neoplasia;
  3. Family history of hereditary CRC;
  4. Abdominal symptoms;
  5. Colectomy;
  6. Severe comorbidity leading to a poor prognosis (life expectancy < 5 years);
  7. Refusal to participate in the study.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

260 participants in 2 patient groups

Fecal occult blood testing
Experimental group
Description:
Annual FIT and colonoscopy in case of a positive test. Fecal occult blood testing: annual FIT (two rounds) without diet restriction, one stool sample. Positive cut-off = 10 μg Hemoglobin/g feces. Colonoscopy will be performed in case of a positive FIT.
Treatment:
Procedure: annual FIT and colonoscopy in case of a positive test
Procedure: colonoscopy with sedation
one-time Colonoscopy
Active Comparator group
Description:
One-time Colonoscopy with sedation
Treatment:
Procedure: colonoscopy with sedation

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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