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Usefulness of Fecal Immunochemical Test in Iron Deficiency Anemia (IDAFIT) (IDAFIT)

Primary Purpose

Colorectal Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Immunochemical fecal occult blood test
Colonoscopy
Upper endoscopy
Sponsored by
Hospital Universitario de Canarias
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Colorectal Cancer focused on measuring Colorectal cancer, Immunochemical occult blood test

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Consecutive outpatients with iron deficiency anemia (Hemoglobin < 13 g/dl in males and 12 g/dl in females) referred for upper endoscopy and/or colonoscopy.
  • To sign the informed consent.

Exclusion Criteria:

  • < 18 years
  • Pregnancy
  • Personal history of inflammatory bowel disease
  • Gastric / duodenal ulcer or gastrointestinal neoplasia
  • Family history of hereditary CRC (Lynch Syndrome or familial adenomatous polyposis)
  • Rectal bleeding / hematochezia
  • Gastroscopy / colonoscopy / endoscopy capsule in the previous 5 years
  • Patients not candidates for endoscopic studies because a low performance status
  • Previous abdominal surgery
  • Refusal to participate.

Sites / Locations

  • Digestive Service, HucRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Colonoscopy followed by upper endoscopy

Upper endoscopy followed by colonoscopy

Arm Description

In case of a positive immunochemical fecal occult blood test result, colonoscopy will be the first examination

In case of a negative immunochemical fecal occult blood test result, upper endoscopy will be the first examination

Outcomes

Primary Outcome Measures

The number of patients with colorectal cancer among those with a positive immunochemical fecal test (Positive predictive value)
In order to calculate the positive predictive value, the number of patients with events (colorectal cancers) will be divided among the number of positive immunochemical fecal tests

Secondary Outcome Measures

The number of patients with a significant lesion among those with a positive immunochemical fecal test (Positive predictive value) after the colonoscopy and after the upper endoscopy
In order to calculate the positive predictive value, the number of patients with a significant lesion (i.e. colorectal cancer, advanced adenoma, inflammatory bowel disease, angiodysplasia, gastric cancer, watermelon stomach, gastric/duodenal ulcer, ampulloma, erosive gastritis/duodenitis) will be divided among the number of positive immunochemical fecal tests.
The number of patients without a significant lesion among those with a negative immunochemical fecal test (negative predictive value) after the colonoscopy and after the upper endoscopy
In order to calculate the negative predictive value, the number of patients without a significant lesion will be divided among patients with a negative immunochemical fecal test

Full Information

First Posted
May 20, 2016
Last Updated
February 17, 2019
Sponsor
Hospital Universitario de Canarias
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1. Study Identification

Unique Protocol Identification Number
NCT02792023
Brief Title
Usefulness of Fecal Immunochemical Test in Iron Deficiency Anemia (IDAFIT)
Acronym
IDAFIT
Official Title
Usefulness of Fecal Immunochemical Test in the Diagnosis Algorithm of Iron Deficiency Anemia.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
June 30, 2016 (Actual)
Primary Completion Date
August 2019 (Anticipated)
Study Completion Date
October 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitario de Canarias

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Prospective study to test whether the immunochemical fecal occult blood test (FIT) for colorectal cancer (CRC) helps to prioritize patients with iron deficiency anemia for colonoscopy.
Detailed Description
This is a multicenter (two centers), prospective study to test the accuracy of FIT for CRC detection in patients with severe IDA and its potential value for prioritizing colonoscopy. An appointment with a gastroenterologist will be scheduled for patients with IDA referred for upper gastrointestinal endoscopy or colonoscopy. The gastroenterologist will check the inclusion and exclusion criteria. Eligible patients will sign the informed consent to carry out the following procedures: Blood analysis to rule out celiac disease (anti-transglutaminase IgA antibodies and IgA). A quantitative fecal immunological test (FIT: OC-Sensor ®) will be provided. An appointment for colonoscopy and gastroscopy will be provided after completion of the FIT in all patients. During gastroscopy, duodenal biopsies from the second portion of the duodenum and duodenal bulb will be taken to rule out celiac disease. Biopsies from the stomach will be also taken to assess helicobacter pylori infection. In patients with severe anemia colonoscopy and upper endoscopy will be prioritized (<20 days) (primary outcome). Patients with colonoscopy and gastroscopy without significant lesions, will be scheduled for the performance of a capsule endoscopy. Endoscopists will be blind for the FIT results. the following information will be collected: consumption of acetylsalicylic acid, non steroidal anti inflammatory drugs, oral anticoagulants, corticosteroids and proton pump inhibitors (PPI). In the case of patients receiving treatment with PPIs, they will be removed 15 days before the completion of the FIT and not resumed until the performance of the upper endoscopy. The hypothesis of the study is that one-time FIT is a useful tool for increasing the efficiency of colonoscopy and can be used to prioritize outpatient colonoscopy in patients with IDA. In order to calculate the sample size required for the study, the investigators have assumed that FIT is positive in 25% of cases with iron deficiency anemia and 20% of them would have an advanced colorectal neoplasia at colonoscopy whereas only 10% of advanced colorectal neoplasias would be found in the remaining 75% patients with a negative FIT. Considering a type I error (alpha) of 5%, a power of 80% and a percentage of losses of 15%, 550 patients will be necessary to include. The investigators estimate that approximately 15% of these patients (n=83) will have severe anemia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Colorectal cancer, Immunochemical occult blood test

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
550 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Colonoscopy followed by upper endoscopy
Arm Type
Other
Arm Description
In case of a positive immunochemical fecal occult blood test result, colonoscopy will be the first examination
Arm Title
Upper endoscopy followed by colonoscopy
Arm Type
Other
Arm Description
In case of a negative immunochemical fecal occult blood test result, upper endoscopy will be the first examination
Intervention Type
Other
Intervention Name(s)
Immunochemical fecal occult blood test
Intervention Description
Participants will be provided with a single immunochemical fecal occult blood test. Participants will introduce a small sample of feces inside and bring the test to the hospital
Intervention Type
Device
Intervention Name(s)
Colonoscopy
Intervention Description
A colonoscopy (procedure performed using a scope design to examine the large bowel) will be offered to the participants
Intervention Type
Device
Intervention Name(s)
Upper endoscopy
Intervention Description
An upper endoscopy (procedure performed using a scope to examine the upper digestive tract) will be offered to the participants
Primary Outcome Measure Information:
Title
The number of patients with colorectal cancer among those with a positive immunochemical fecal test (Positive predictive value)
Description
In order to calculate the positive predictive value, the number of patients with events (colorectal cancers) will be divided among the number of positive immunochemical fecal tests
Time Frame
one year
Secondary Outcome Measure Information:
Title
The number of patients with a significant lesion among those with a positive immunochemical fecal test (Positive predictive value) after the colonoscopy and after the upper endoscopy
Description
In order to calculate the positive predictive value, the number of patients with a significant lesion (i.e. colorectal cancer, advanced adenoma, inflammatory bowel disease, angiodysplasia, gastric cancer, watermelon stomach, gastric/duodenal ulcer, ampulloma, erosive gastritis/duodenitis) will be divided among the number of positive immunochemical fecal tests.
Time Frame
one year
Title
The number of patients without a significant lesion among those with a negative immunochemical fecal test (negative predictive value) after the colonoscopy and after the upper endoscopy
Description
In order to calculate the negative predictive value, the number of patients without a significant lesion will be divided among patients with a negative immunochemical fecal test
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Consecutive outpatients with iron deficiency anemia (Hemoglobin < 13 g/dl in males and 12 g/dl in females) referred for upper endoscopy and/or colonoscopy. To sign the informed consent. Exclusion Criteria: < 18 years Pregnancy Personal history of inflammatory bowel disease Gastric / duodenal ulcer or gastrointestinal neoplasia Family history of hereditary CRC (Lynch Syndrome or familial adenomatous polyposis) Rectal bleeding / hematochezia Gastroscopy / colonoscopy / endoscopy capsule in the previous 5 years Patients not candidates for endoscopic studies because a low performance status Previous abdominal surgery Refusal to participate.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marta Carrillo, MD, PhD
Phone
34-922678000
Ext
34039
Email
martacarry@yahoo.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enrique Quintero, MD, PhD
Organizational Affiliation
Hospital Universitario de Canarias
Official's Role
Study Director
Facility Information:
Facility Name
Digestive Service, Huc
City
La Laguna
State/Province
S/C DE Tenerife
ZIP/Postal Code
38320
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ENRIQUE QUINTERO, MD. PhD.
Phone
615553711
Email
equintero@gmail.com
First Name & Middle Initial & Last Name & Degree
ENRIQUE QUINTERO, MD. PhD.
First Name & Middle Initial & Last Name & Degree
Antonio Z Gimeno García, MD PhD
First Name & Middle Initial & Last Name & Degree
Zaida Adrián de Ganzo, MD PhD
First Name & Middle Initial & Last Name & Degree
David N Pérez, MD PhD
First Name & Middle Initial & Last Name & Degree
Marta Carrillo Palau, MD PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
16215432
Citation
James MW, Chen CM, Goddard WP, Scott BB, Goddard AF. Risk factors for gastrointestinal malignancy in patients with iron-deficiency anaemia. Eur J Gastroenterol Hepatol. 2005 Nov;17(11):1197-203. doi: 10.1097/00042737-200511000-00008.
Results Reference
background
PubMed Identifier
18219289
Citation
Hamilton W, Lancashire R, Sharp D, Peters TJ, Cheng KK, Marshall T. The importance of anaemia in diagnosing colorectal cancer: a case-control study using electronic primary care records. Br J Cancer. 2008 Jan 29;98(2):323-7. doi: 10.1038/sj.bjc.6604165. Epub 2008 Jan 22.
Results Reference
background
PubMed Identifier
22356323
Citation
Quintero E, Castells A, Bujanda L, Cubiella J, Salas D, Lanas A, Andreu M, Carballo F, Morillas JD, Hernandez C, Jover R, Montalvo I, Arenas J, Laredo E, Hernandez V, Iglesias F, Cid E, Zubizarreta R, Sala T, Ponce M, Andres M, Teruel G, Peris A, Roncales MP, Polo-Tomas M, Bessa X, Ferrer-Armengou O, Grau J, Serradesanferm A, Ono A, Cruzado J, Perez-Riquelme F, Alonso-Abreu I, de la Vega-Prieto M, Reyes-Melian JM, Cacho G, Diaz-Tasende J, Herreros-de-Tejada A, Poves C, Santander C, Gonzalez-Navarro A; COLONPREV Study Investigators. Colonoscopy versus fecal immunochemical testing in colorectal-cancer screening. N Engl J Med. 2012 Feb 23;366(8):697-706. doi: 10.1056/NEJMoa1108895. Erratum In: N Engl J Med. 2016 May 12;374(19):1898.
Results Reference
background
PubMed Identifier
25127679
Citation
Quintero E, Carrillo M, Gimeno-Garcia AZ, Hernandez-Guerra M, Nicolas-Perez D, Alonso-Abreu I, Diez-Fuentes ML, Abraira V. Equivalency of fecal immunochemical tests and colonoscopy in familial colorectal cancer screening. Gastroenterology. 2014 Nov;147(5):1021-30.e1; quiz e16-7. doi: 10.1053/j.gastro.2014.08.004. Epub 2014 Aug 13.
Results Reference
background
PubMed Identifier
26055489
Citation
Rodriguez-Alonso L, Rodriguez-Moranta F, Ruiz-Cerulla A, Lobaton T, Arajol C, Binefa G, Moreno V, Guardiola J. An urgent referral strategy for symptomatic patients with suspected colorectal cancer based on a quantitative immunochemical faecal occult blood test. Dig Liver Dis. 2015 Sep;47(9):797-804. doi: 10.1016/j.dld.2015.05.004. Epub 2015 May 15.
Results Reference
background
PubMed Identifier
24456168
Citation
Cubiella J, Salve M, Diaz-Ondina M, Vega P, Alves MT, Iglesias F, Sanchez E, Macia P, Blanco I, Bujanda L, Fernandez-Seara J. Diagnostic accuracy of the faecal immunochemical test for colorectal cancer in symptomatic patients: comparison with NICE and SIGN referral criteria. Colorectal Dis. 2014 Aug;16(8):O273-82. doi: 10.1111/codi.12569.
Results Reference
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Usefulness of Fecal Immunochemical Test in Iron Deficiency Anemia (IDAFIT)

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