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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04242901
Other study ID # 19ON031
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 20, 2020
Est. completion date February 7, 2023

Study information

Verified date May 2023
Source Nottingham University Hospitals NHS Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Assimilation of FIT into primary and secondary care diagnostic pathways will lead to an increased prominence of the investigation in the diagnosis of colorectal cancer (CRC). Questions remain about whether serial FIT analysis improves accuracy, and what factors affect it. Our study will analyse FIT results in recently diagnosed CRC patients to determine the risk of a false-negative FIT result and evaluate whether repeated analysis improves diagnostic accuracy. The study aims to advise on whether there is an optimal interval between sample collection to improve diagnostic accuracy and whether any patients are at risk of a false negative based on demographics, medications or other pathological factors.


Description:

Colorectal cancer (CRC) remains a leading cause of cancer death in the UK and worldwide. Improving outcomes depends in part on achieving earlier diagnosis of the disease. The Faecal Immunochemical Test (FIT) is replacing the less accurate Faecal Occult Blood Test (FOBT) in the UK and has the potential to help achieve earlier stage diagnosis of CRC. Whilst FIT has been validated as a screening test for the Bowel Cancer Screening Programme (BCSP), its role in diagnosing CRC in symptomatic populations is yet to be defined. Nottingham is a pioneering centre using FIT to stratify risk and determine first-investigation in its two-week-wait (2WW) pathway. To optimise use of FIT and minimise the chance of missed cancers, this project aims to better understand variation of FIT results over time and how certain factors affect FIT result. Much of the literature has focused on the evaluation of FIT in an asymptomatic population, which is inherently low risk (4,6,7). Expanding use of FIT to stratify risk and guide investigations for cancer in (higher risk) symptomatic populations necessitates a thoroughly evaluated testing strategy. At present there is insufficient information to advise on "negative" FIT results in symptomatic patients. This study will comprehensively measure FIT variation over time in patients with the target condition (CRC) and help answer whether additional samples are likely to improve accuracy of FIT. Risk factors for false positives and false negatives have been previously identified but are not widely established (4). Our study will record the presence of these risk factors, and evaluate their effects on FIT-positivity with subsequent statistical analysis.


Recruitment information / eligibility

Status Completed
Enrollment 58
Est. completion date February 7, 2023
Est. primary completion date February 7, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Histologically confirmed colorectal cancer Exclusion Criteria: - Less than 18 years old - Not attending Nottingham University Hospitals for diagnosis/treatment (attending another trust) - No histological diagnosis of colorectal cancer - Unable to provide informed consent - for example due to language barriers or lacking capacity to join study

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Faecal Immunochemical Test - OC Sensor, Eiken, Tokyo
Quantitative Faecal Immunochemical Test - OC Sensor, Eiken, Tokyo

Locations

Country Name City State
United Kingdom Queens Medical Centre Nottingham Nottinghamshire

Sponsors (1)

Lead Sponsor Collaborator
Nottingham University Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary False negative FIT results - Determine the occurrence of falsely negative FIT results in the presence of colorectal cancer Determine the occurrence of falsely negative FIT results in the presence of colorectal cancer 2 years
Primary Number of participants who yield sequential FIT results in divergent strata used for clinical decision making Number of participants who yield sequential FIT results in divergent strata used for clinical decision making (FIT <4 µg Hb/g faeces, 4-9.9 µg Hb/g faeces, 10-99.9 µg Hb/g faeces, 100-150 µg Hb/g faeces, >150 µg Hb/g faeces) 2 years
Secondary Calculation of Odds Ratios for age, gender, family history of CRC, hypertension, obesity, smoking status, excessive alcohol intake, right sided tumour, stage 1 cancer Calculation of Odds Ratios for age, gender, family history of CRC, hypertension, obesity, smoking status, excessive alcohol intake, right sided tumour, stage 1 cancer 2 years
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