Colorectal AdenomaOSCARNCT03663062
ObeSity Related Colorectal Adenoma Risk
An observational study of Colorectal Adenoma and Colorectal Neoplasm, run by South Tyneside and Sunderland NHS Foundation Trust at 12 sites in United Kingdom.
Trial summary
In the UK, around 1 in 16 men and 1 in 20 women will develop bowel cancer at some point in their lives. Most bowel cancers happen when a type of growth in the bowel called an adenoma eventually becomes cancerous. Cutting out adenomas reduces the risk of developing bowel cancer. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Colorectal Adenoma, Colorectal Neoplasm, Colorectal Cancer
- What is being tested?
- Colonoscopy
- How many people
- 1,430 participants
- Where
- 12 sitesUnited Kingdom
- Study dates
- 27 Dec 2017to 7 Jun 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Any patient referred for colonoscopy matching the inclusion and exclusion criteria
Who may be able to join
- Aged 18 years and over
- Able to give informed consent
- Indications:
- Patients with positive faecal occult blood test (FOBt) referred for index colonoscopy as part of Bowel Cancer Screening Programme
- Colonoscopy conversion from Bowelscope
- Index diagnostic colonoscopy due to new gastrointestinal symptoms (including but not restricted to diarrhoea, change in bowel habit, abdominal pain, PR bleeding, weight loss), iron deficiency anaemia, family history of CRC, abnormal findings on cross sectional imaging
Who cannot join
- Absolute contraindication to colonoscopy
- Unable to give informed consent
- Known colorectal cancer
- Known polyposis syndrome
- Previous total/subtotal colectomy
- Known colonic stricture which would prevent completion of colonoscopy
Show all 11Show fewer
- Attending for therapeutic procedure
- Attending for assessment of a known lesion
- Attending for assessment of known inflammatory bowel disease (IBD)
- Attending for surveillance colonoscopy (polyp surveillance, post colorectal cancer surveillance, IBD surveillance)
- Colonoscopy within the last 5 years
Trial locations and contacts
12 sites in 1 country.
12 sites in 1 country
United Kingdom12 sites
Blackpool Teaching Hospitals NHS Foundation Trust
Blackpool
Royal Bolton Hospital
Bolton, Greater Manchaster, BL4 0JR
Mid Cheshire Hospitals NHS Foundation Trust
Crewe, Mid Cheshire, CW1 4QJ
Gloucestershire Hospitals NHS Foundation Trust
Gloucester, GL1 3NN
Kettering General Hospitals NHS Foundation Trust
Kettering, NN16 8UZ
University Hospitals of Morecambe Bay NHS Foundation Trust
Lancaster, Lancashire, LA1 4RP
South Tees Hospitals NHS Foundation Trust
Middlesbrough, TS4 3BW
Newcastle Upon Tyne NHS Foundation Trust
Newcastle upon Tyne, NE7 7DN
Lancashire Teaching Hospitals NHS Foundation Trust
Preston, PR25BW
South Tyneside NHS Foundation Trust
South Shields, Tyne and Wear, NE34 0PL
North Tees and Hartlepool NHS Foundation Trust
Stockton-on-Tees, TS19 8PE
CIty Hospitals Sunderland NHS Foundation Trust
Sunderland, SR4 7TP
About this study
In the UK, around 1 in 16 men and 1 in 20 women will develop bowel cancer at some point in their lives. Most bowel cancers happen when a type of growth in the bowel called an adenoma eventually becomes cancerous. Cutting out adenomas reduces the risk of developing bowel cancer.
Certain people are more likely to have adenomas than others, for example people who are overweight. People who are overweight are also more likely to develop liver disease by laying too much fat down in the liver. Studies in Asia have shown that people with fatty liver disease are more likely to have adenomas and these are more commonly found in the part of the bowel (right colon) furthest from the bottom end.
Read more
Information on the link between obesity, fatty liver disease and adenomas is very limited, particularly in the Western population.
The investigators will assess the link between body weight, fatty liver and adenomas in the UK population. 1430 patients will be invited; some through the bowel cancer screening programme and some with symptoms such as low blood count, bleeding or changed bowel habit. These patients will already have been referred for a camera test looking into the bowel, called a colonoscopy. Information including height, weight and some health questions will be taken. Blood samples will be taken. The investigators will compare the number of patients with adenomas who have liver disease or who are overweight with those who don't. This information will be used to develop a scoring system to predict risk of adenomas. This will help the investigators to decide if undertaking colonoscopies in these patients will identify those at increased risk of bowel cancer.
Read the detailed description
Bowel cancer, or colorectal cancer (CRC), is the second most common cancer affecting both men and women in England. The majority of CRCs develop from a pre-cancerous type of growth in the bowel called an adenoma. Detecting and removing these adenomas is important in reducing CRC risk. A study which undertook a once-off camera examination of the left hand side of the bowel (flexible sigmoidoscopy), removing any adenomas, demonstrated a reduction in CRC by 23% and reduced mortality by 31%.
Although a single cause for adenomas is not known, several factors can predispose patients to adenomas, including; age, gender, family history, cigarette smoking and excess body weight (EBW).
Obesity is becoming an increasing problem in the UK, with approximately a quarter of adults classed as obese in England. Patients who are obese are at higher risk of having adenomas. Studies have shown that patients with EBW are more likely to have fatty disease of the liver (non-alcoholic fatty liver disease, NAFLD) by laying down fat in the liver. Studies in Asia have shown that patients with NAFLD are more likely to have adenomas, and that these are more likely to be in the right side of the bowel which is furthest from the anus (right colon). Although these studies have shown a link between NAFLD and adenomas, they have all used invasive or expensive markers of fatty liver disease. No study has correlated the link between liver enzymes (blood tests) and adenomas or by using scoring systems to determine the presence or absence of significant fatty liver disease. Furthermore, no Western studies have confirmed the link between NAFLD and adenomas, meaning it is unclear whether this link is only present in the Asian population.
Approximately 400,000 colonoscopies (camera examinations of the large bowel) are performed each year within the NHS for the investigation of gastrointestinal symptoms, including: altered bowel habit, rectal bleeding and low blood count. When polyps are found, patients often have a follow-up surveillance colonoscopy to check that no new adenomas have formed. The timing and need for surveillance is based only on the number and size of adenomas found and does not take into account any risk factors which the patient may have.
The NHS Bowel Cancer Screening Programme (BCSP) invites all individuals aged 60-74 to undertake a stool sample test which looks for blood, called faecal occult blood testing (FOBt), every two years. Those who have a positive FOBt are then invited for a colonoscopy. This programme is purely based on age and is not targeted. Another arm of the BCSP was introduced in 2013, where all individuals aged 55 are invited for a flexible sigmoidoscopy and removal of adenomas. Anyone who is felt to be high risk according to the number or size of adenomas then undergoes a colonoscopy.
The BCSP has led to cancers being detected at an earlier stage, but is not protecting the population against cancers in the right side of the bowel.
In summary, although studies in Asian populations have suggested an association between NAFLD and colorectal adenomas, this has not been repeated in a Western population. It is important that the association is explored further in a Western population, in a simple, non-invasive manner. Assessing markers of NAFLD and a wider range of risk factors for adenomas will allow us to develop a tool to predict which patients are at increased risk of adenomas, called a risk model.
The OSCAR study is a multicentre observational study has been designed which will recruit 1430 participants from nine sites, eight in the North of England who are all members of the Northern Region Endoscopy Group (NREG) and one from Kettering General Hospital NHS Trust. NREG is an endoscopy research collaborative group with an excellent track record of delivering similar endoscopy based research studies to time and target. Participation will involve collecting information relating to obesity and fatty liver disease in patients already attending for colonoscopy in addition to collecting information about the number and size of any adenomas found.
All patients scheduled for colonoscopy will be provided with an invitation letter and patient information sheet in addition with the standard information about the colonoscopy procedure that the endoscopy unit provides. As colonoscopy requires a period of preparation prior to the test, patients will receive this information at least 24 hours before the procedure, allowing ample time to consider the study before attending the endoscopy department.
Taking part in this study will change very little about the patients' experience of the colonoscopy test itself. If the patient agrees to take part in this study, the information sheet will be reviewed with them by a research team member, an opportunity to ask questions given, and the consent form signed. Eligibility to take part in the study will be checked, and the patient will be weighed, have their height checked, waist circumference measured, body mass index (BMI) calculated and blood pressure checked. A research team member will undertake a health questionnaire which will include the following items:
- Current and previous smoking history
- Current and previous alcohol history
- Current medications: including Aspirin, Statin, Insulin, non-steroidal anti-inflammatory drugs (NSAIDs), Diabetic medication, antibiotics and others
- Family history of colorectal cancer
- Family history of ischaemic heart disease in a first degree relative under the age of 60
- History of liver disease
- History of hypertension
- History of diabetes- Type I, Type II
- History of chronic kidney disease (Stage 4/5)
- History of atrial fibrillation
- History of rheumatoid arthritis
- Personal history of anti-obesity surgery
These will be entered onto the case report form (CRF).
An intravenous cannula (a thin, plastic tube which is inserted into a vein in the arm) is then inserted as part of routine care before the colonoscopy procedure. Blood tests will be taken from this at the time of insertion to prevent the need for a separate blood test. These tests will include:
- Bilirubin
- Alanine aminotransferase (ALT)
- Alkaline phosphatase (ALP)
- Aspartate aminotransferase (AST)
- Gamma-glutamyl transferase (GGT)
- Full blood count (FBC)
- HbA1c
- Fasting blood glucose
- Lipids: Cholesterol, HDL and Triglycerides
- Albumin
- Immunoglobulin A
Patients will also need to sign a separate consent form for the colonoscopy procedure itself as part of routine practice.
The patient will then enter the procedure room as per usual practice for their colonoscopy. During the procedure, the research team member will record data onto the CRF (procedural data, findings at colonoscopy etc). The colonoscopy report will be generated as per the usual practice in each unit.
A subset of patients will undergo Fibroscan, which is a non-invasive test to evaluate for liver fibrosis, to explore the association between the presence of colorectal adenoma/CRC and the presence of liver fibrosis.
After the procedure, the patient will enter the recovery ward and follow usual practice in the unit. Although participants will remain in the study for 14 days to allow data collection and to follow-up any abnormal results, participants will not require any further visits and the majority will not be contacted by the research team. If a new abnormality is found on checking blood samples, the patient will be contacted by a member of the research team and advised to make an appointment with their General Practitioner (GP).
Statistical analysis will be undertaken by Professor Steven Rushton, Professor of Biological Modelling at Newcastle University.
The primary outcome of this study is to develop a risk model which can be used to inform colorectal neoplasia screening and surveillance guidelines and to inform a future study targeting screening of higher risk individuals.
The secondary outcomes will support this model by identifying which demographics contribute to increased predisposition to colorectal neoplasia, namely smoking history, alcohol intake, and obesity (measured by BMI and waist circumference). The investigators also aim to assess whether the presence or degree of liver fibrosis, as measured by FIB4 score and Fibroscan affects the risk of colorectal neoplasia and by exploring the link between NAFLD, obesity and colorectal neoplasia in terms of adenoma burden, site and histological features. Lastly, the association between abnormal liver enzymes and colorectal neoplasia will be explored.
- Conditions
- Colorectal Adenoma, Colorectal Neoplasm, Colorectal Cancer, Obesity, Metabolic Syndrome, Non-Alcoholic Fatty Liver Disease
- Being tested
- Colonoscopy
- Keywords
- colorectal adenoma, colorectal cancer, Obesity, Non-Alcoholic Fatty Liver Disease, Metabolic syndrome, Liver Fibrosis
- Medical subject headings
- Colorectal Neoplasms, Obesity, Metabolic Syndrome, Non-alcoholic Fatty Liver Disease, Liver Cirrhosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ColonoscopyDiagnostic test
Also called Blood tests, Fibroscan, BMI measurement, Waist circumference measurement
All patients would undergo colonoscopy as part of standard care. Patients recruited for this study would have their past medical history, family history, medication history, as well as waist circumference, BMI and blood pressure recorded. All patients would also have blood tests (described earlier) and a subset will undergo Fibroscan.
What is being measured
The primary outcome is the main question the study is designed to answer.
Risk model of colorectal adenomas and CRC
Risk prediction model
Measured: 24 months from patient recruitment
Secondary outcomes (5)
The incidence of colorectal adenomas or CRC in patients with abnormal liver enzymes
Number of patients with colorectal adenomas or CRC who have abnormal liver enzymes
Measured: 24 months from patient recruitment
The incidence colorectal adenomas or CRC in patients with obesity
Number of patients with colorectal adenomas or CRC who are obese, as measured by BMI or waist circumference
Measured: 24 months from patient recruitment
The incidence colorectal adenomas or CRC in patients with abnormal FIB4 score
Number of patients with colorectal adenomas or CRC who have abnormal FIB4 score
Measured: 24 months from patient recruitment
The incidence colorectal adenomas or CRC in patients with abnormal Fibroscan readings
Number of patients with colorectal adenomas or CRC who have abnormal Fibroscan readings
Measured: 24 months from patient recruitment
The incidence of colorectal adenomas or CRC in patients who are smokers or who have high alcohol intake
Number of patients with colorectal adenomas or CRC who are smokers or have high alcohol intake
Measured: 24 months from patient recruitment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Sep 2018
- Study start27 Dec 2017
- Primary completion7 Jun 2019
- Study completion7 Jun 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Colorectal AdenomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,430 participants (actual)
Sponsor and investigators
- Lead sponsor
- South Tyneside and Sunderland NHS Foundation Trust
- Sponsor type
- University, hospital or other
- Collaborators
- Newcastle-upon-Tyne Hospitals NHS Trust, City Hospitals Sunderland NHS Foundation Trust, North Tees and Hartlepool NHS Foundation Trust, South Tees Hospitals NHS Foundation Trust, Kettering General Hospital NHS Foundation Trust, Royal Bolton Hospital NHS Foundation Trust, Gloucestershire Hospitals NHS Foundation Trust, University Hospitals of Morecambe Bay NHS Trust, Mid Cheshire Hospitals NHS Foundation Trust, Lancashire Teaching Hospitals NHS Foundation Trust, Blackpool Teaching Hospitals NHS Foundation Trust
- Responsible party
- Sponsor
- Investigators
- Colin Rees, FRCP, Principal investigator, South Tyneside and Sunderland NHS Foundation Trust
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03663062
- Sponsor's protocol ID
- OSCAR
- Acronym
- OSCAR
- Status last verified
- Sep 2018
- First submitted
- 15 Dec 2017
- Last updated
- 4 Nov 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: There are no plans for this at present
Study at a glance
From the registry record, last updated by the sponsor on 4 Nov 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- ObeSity Related Colorectal Adenoma Risk
- ClinicalTrials.gov ID
- NCT03663062
- Acronym / sponsor ID
- OSCAR / OSCAR
- Conditions
- Colorectal Adenoma, Colorectal Neoplasm, Colorectal Cancer, Obesity, Metabolic Syndrome, Non-Alcoholic Fatty Liver Disease
- Keywords
- colorectal adenoma, colorectal cancer, Obesity, Non-Alcoholic Fatty Liver Disease, Metabolic syndrome, Liver Fibrosis
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,430 participants (actual)
- Lead sponsor
- South Tyneside and Sunderland NHS Foundation TrustUniversity, hospital or other
- Collaborators
- Newcastle-upon-Tyne Hospitals NHS Trust, City Hospitals Sunderland NHS Foundation Trust, North Tees and Hartlepool NHS Foundation Trust, South Tees Hospitals NHS Foundation Trust, Kettering General Hospital NHS Foundation Trust, Royal Bolton Hospital NHS Foundation Trust, Gloucestershire Hospitals NHS Foundation Trust, University Hospitals of Morecambe Bay NHS Trust, Mid Cheshire Hospitals NHS Foundation Trust, Lancashire Teaching Hospitals NHS Foundation Trust, Blackpool Teaching Hospitals NHS Foundation Trust
- Study start
- 27 Dec 2017 (actual)
- Primary completion
- 7 Jun 2019 (actual)
- Study completion
- 7 Jun 2019 (actual)
- First posted
- 10 Sep 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In the UK, around 1 in 16 men and 1 in 20 women will develop bowel cancer at some point in their lives. Most bowel cancers happen when a type of growth in the bowel called an adenoma eventually becomes cancerous. Cutting out adenomas reduces the risk of developing bowel cancer.
Certain people are more likely to have adenomas than others, for example people who are overweight. People who are overweight are also more likely to develop liver disease by laying too much fat down in the liver. Studies in Asia have shown that people with fatty liver disease are more likely to have adenomas and these are more commonly found in the part of the bowel (right colon) furthest from the bottom end.
Information on the link between obesity, fatty liver disease and adenomas is very limited, particularly in the Western population.
The investigators will assess the link between body weight, fatty liver and adenomas in the UK population. 1430 patients will be invited; some through the bowel cancer screening programme and some with symptoms such as low blood count, bleeding or changed bowel habit. These patients will already have been referred for a camera test looking into the bowel, called a colonoscopy. Information including height, weight and some health questions will be taken. Blood samples will be taken. The investigators will compare the number of patients with adenomas who have liver disease or who are overweight with those who don't. This information will be used to develop a scoring system to predict risk of adenomas. This will help the investigators to decide if undertaking colonoscopies in these patients will identify those at increased risk of bowel cancer.
Detailed description
Bowel cancer, or colorectal cancer (CRC), is the second most common cancer affecting both men and women in England. The majority of CRCs develop from a pre-cancerous type of growth in the bowel called an adenoma. Detecting and removing these adenomas is important in reducing CRC risk. A study which undertook a once-off camera examination of the left hand side of the bowel (flexible sigmoidoscopy), removing any adenomas, demonstrated a reduction in CRC by 23% and reduced mortality by 31%.
Although a single cause for adenomas is not known, several factors can predispose patients to adenomas, including; age, gender, family history, cigarette smoking and excess body weight (EBW).
Obesity is becoming an increasing problem in the UK, with approximately a quarter of adults classed as obese in England. Patients who are obese are at higher risk of having adenomas. Studies have shown that patients with EBW are more likely to have fatty disease of the liver (non-alcoholic fatty liver disease, NAFLD) by laying down fat in the liver. Studies in Asia have shown that patients with NAFLD are more likely to have adenomas, and that these are more likely to be in the right side of the bowel which is furthest from the anus (right colon). Although these studies have shown a link between NAFLD and adenomas, they have all used invasive or expensive markers of fatty liver disease. No study has correlated the link between liver enzymes (blood tests) and adenomas or by using scoring systems to determine the presence or absence of significant fatty liver disease. Furthermore, no Western studies have confirmed the link between NAFLD and adenomas, meaning it is unclear whether this link is only present in the Asian population.
Approximately 400,000 colonoscopies (camera examinations of the large bowel) are performed each year within the NHS for the investigation of gastrointestinal symptoms, including: altered bowel habit, rectal bleeding and low blood count. When polyps are found, patients often have a follow-up surveillance colonoscopy to check that no new adenomas have formed. The timing and need for surveillance is based only on the number and size of adenomas found and does not take into account any risk factors which the patient may have.
The NHS Bowel Cancer Screening Programme (BCSP) invites all individuals aged 60-74 to undertake a stool sample test which looks for blood, called faecal occult blood testing (FOBt), every two years. Those who have a positive FOBt are then invited for a colonoscopy. This programme is purely based on age and is not targeted. Another arm of the BCSP was introduced in 2013, where all individuals aged 55 are invited for a flexible sigmoidoscopy and removal of adenomas. Anyone who is felt to be high risk according to the number or size of adenomas then undergoes a colonoscopy.
The BCSP has led to cancers being detected at an earlier stage, but is not protecting the population against cancers in the right side of the bowel.
In summary, although studies in Asian populations have suggested an association between NAFLD and colorectal adenomas, this has not been repeated in a Western population. It is important that the association is explored further in a Western population, in a simple, non-invasive manner. Assessing markers of NAFLD and a wider range of risk factors for adenomas will allow us to develop a tool to predict which patients are at increased risk of adenomas, called a risk model.
The OSCAR study is a multicentre observational study has been designed which will recruit 1430 participants from nine sites, eight in the North of England who are all members of the Northern Region Endoscopy Group (NREG) and one from Kettering General Hospital NHS Trust. NREG is an endoscopy research collaborative group with an excellent track record of delivering similar endoscopy based research studies to time and target. Participation will involve collecting information relating to obesity and fatty liver disease in patients already attending for colonoscopy in addition to collecting information about the number and size of any adenomas found.
All patients scheduled for colonoscopy will be provided with an invitation letter and patient information sheet in addition with the standard information about the colonoscopy procedure that the endoscopy unit provides. As colonoscopy requires a period of preparation prior to the test, patients will receive this information at least 24 hours before the procedure, allowing ample time to consider the study before attending the endoscopy department.
Taking part in this study will change very little about the patients' experience of the colonoscopy test itself. If the patient agrees to take part in this study, the information sheet will be reviewed with them by a research team member, an opportunity to ask questions given, and the consent form signed. Eligibility to take part in the study will be checked, and the patient will be weighed, have their height checked, waist circumference measured, body mass index (BMI) calculated and blood pressure checked. A research team member will undertake a health questionnaire which will include the following items:
- Current and previous smoking history
- Current and previous alcohol history
- Current medications: including Aspirin, Statin, Insulin, non-steroidal anti-inflammatory drugs (NSAIDs), Diabetic medication, antibiotics and others
- Family history of colorectal cancer
- Family history of ischaemic heart disease in a first degree relative under the age of 60
- History of liver disease
- History of hypertension
- History of diabetes- Type I, Type II
- History of chronic kidney disease (Stage 4/5)
- History of atrial fibrillation
- History of rheumatoid arthritis
- Personal history of anti-obesity surgery
These will be entered onto the case report form (CRF).
An intravenous cannula (a thin, plastic tube which is inserted into a vein in the arm) is then inserted as part of routine care before the colonoscopy procedure. Blood tests will be taken from this at the time of insertion to prevent the need for a separate blood test. These tests will include:
- Bilirubin
- Alanine aminotransferase (ALT)
- Alkaline phosphatase (ALP)
- Aspartate aminotransferase (AST)
- Gamma-glutamyl transferase (GGT)
- Full blood count (FBC)
- HbA1c
- Fasting blood glucose
- Lipids: Cholesterol, HDL and Triglycerides
- Albumin
- Immunoglobulin A
Patients will also need to sign a separate consent form for the colonoscopy procedure itself as part of routine practice.
The patient will then enter the procedure room as per usual practice for their colonoscopy. During the procedure, the research team member will record data onto the CRF (procedural data, findings at colonoscopy etc). The colonoscopy report will be generated as per the usual practice in each unit.
A subset of patients will undergo Fibroscan, which is a non-invasive test to evaluate for liver fibrosis, to explore the association between the presence of colorectal adenoma/CRC and the presence of liver fibrosis.
After the procedure, the patient will enter the recovery ward and follow usual practice in the unit. Although participants will remain in the study for 14 days to allow data collection and to follow-up any abnormal results, participants will not require any further visits and the majority will not be contacted by the research team. If a new abnormality is found on checking blood samples, the patient will be contacted by a member of the research team and advised to make an appointment with their General Practitioner (GP).
Statistical analysis will be undertaken by Professor Steven Rushton, Professor of Biological Modelling at Newcastle University.
The primary outcome of this study is to develop a risk model which can be used to inform colorectal neoplasia screening and surveillance guidelines and to inform a future study targeting screening of higher risk individuals.
The secondary outcomes will support this model by identifying which demographics contribute to increased predisposition to colorectal neoplasia, namely smoking history, alcohol intake, and obesity (measured by BMI and waist circumference). The investigators also aim to assess whether the presence or degree of liver fibrosis, as measured by FIB4 score and Fibroscan affects the risk of colorectal neoplasia and by exploring the link between NAFLD, obesity and colorectal neoplasia in terms of adenoma burden, site and histological features. Lastly, the association between abnormal liver enzymes and colorectal neoplasia will be explored.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Any patient referred for colonoscopy matching the inclusion and exclusion criteria
Key inclusion criteria (6 listed)
- Aged 18 years and over
- Able to give informed consent
- Indications:
Key exclusion criteria (11 listed)
- Absolute contraindication to colonoscopy
- Unable to give informed consent
- Known colorectal cancer
- Known polyposis syndrome
- Previous total/subtotal colectomy
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ColonoscopyAlso: Blood tests, Fibroscan, BMI measurement, Waist circumference measurementAll patients would undergo colonoscopy as part of standard care. Patients recruited for this study would have their past medical history, family history, medication history, as well as waist circumference, BMI and blood pressure recorded. All patients would also have blood tests (described earlier) and a subset will undergo Fibroscan. | Diagnostic test | – |
Primary outcome
Risk model of colorectal adenomas and CRC
Time frame: 24 months from patient recruitment
Risk prediction model
5 secondary outcomes
The incidence of colorectal adenomas or CRC in patients with abnormal liver enzymes
Time frame: 24 months from patient recruitment
The incidence colorectal adenomas or CRC in patients with obesity
Time frame: 24 months from patient recruitment
The incidence colorectal adenomas or CRC in patients with abnormal FIB4 score
Time frame: 24 months from patient recruitment
The incidence colorectal adenomas or CRC in patients with abnormal Fibroscan readings
Time frame: 24 months from patient recruitment
The incidence of colorectal adenomas or CRC in patients who are smokers or who have high alcohol intake
Time frame: 24 months from patient recruitment
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Nov 2020.
- Individual participant dataSharing planned: No. There are no plans for this at present
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Colin Rees, FRCP principal investigator
South Tyneside and Sunderland NHS Foundation Trust
12 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Colorectal Adenoma and Colorectal Neoplasm, run by South Tyneside and Sunderland NHS Foundation Trust at 12 sites in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Nov 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 12 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Risk model of colorectal adenomas and CRC (time frame: 24 months from patient recruitment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Nov 2020.