Cholecystitis; Acute, CholedocholithiasisE-MAGEDNCT03709030
Early MRI in Acute GallstonE Disease
A study testing magnetic resonance cholangiopancreatography (MRCP) in people with Cholecystitis; Acute, Choledocholithiasis, run by Perspectum at 1 site in United Kingdom.
Trial summary
This pilot study aims to determine the utility of direct Magnetic Resonance Cholangiopancreatography (MRCP) in the assessment of suspected acute gallstone disease presentations. This will take the form of a randomized controlled trial, the design of which is based on recent internal audit data which indicated that a… Read more about this study
- Who is it for?
- Ages 16 years and older
- Conditions the study is for
- Cholecystitis; Acute, Choledocholithiasis
- What is being tested?
- magnetic resonance cholangiopancreatography (MRCP)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 27 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 17 Jul 2019to 31 Dec 2020
- Phase
- Interventional
- 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 16 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Participant is willing and able to give informed consent for participation in the study.
- Male or Female, aged 16 years or above.
- Suspected gallstone/biliary disease presenting with acute abdominal pain AND
- At least one of the following blood test results to reflect abnormal liver function;
- Bilirubin > 23 IU/L
- Alanine Aminotransferase > 50 IU/L
Show all 9Show fewer
- Aspartate Aminotransferase >46 IU/L
- Gamma Glutamyl Transpeptidase > 44 IU/L
- Amylase > 138 IU/L
Who cannot join
- Pregnant or nursing (lactating) women
- Previous diagnosis of chronic pancreatitis/hepatitis or chronic alcohol abuse
- Patients with contraindications to MR imaging
- Unstable disease as per judgment of the investigator which would render the patient unsuitable for MR imaging
- If not suitable for study intervention on admission - e.g. requiring immediate ERCP/surgery, or ICU admission
- Previous enrolment in the study (i.e. on repeat attendance to hospital)
- Already admitted to hospital for more than 16 hours
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site
Oxford University Hospitals NHS Foundation Trust
Oxford, Oxfordshire, OX3 9DU
About this study
Official title: Determining the Utility of Direct Access Magnetic Resonance Cholangiopancreatography (MRCP) in the Assessment of Suspected Acute Gallstone Disease Presentations
This pilot study aims to determine the utility of direct Magnetic Resonance Cholangiopancreatography (MRCP) in the assessment of suspected acute gallstone disease presentations. This will take the form of a randomized controlled trial, the design of which is based on recent internal audit data which indicated that a high proportion of patients ultimately require MRCP prior to diagnosis, treatment and discharge, and suggested that early scan may improve overall costs and outcomes. Patients with symptoms and signs suggestive of suspected gallstone disease and deranged liver function tests/amylase (i.e. suggestive of a potentially obstructive gallstone disease), will be enrolled across the full range of 'front-door' locations for surgical presentations within the hospital (Emergency Department, Surgical Emergency Unit, Ambulatory Assessment Unit), and randomized to one of two diagnostic pathways which are both existing variations in current clinical care:
- MRCP is used as the first mode of imaging;
- following a standard care model (ultrasound then MRCP if deemed appropriate). An assessment will then be undertaken of the cost-effectiveness of early MRCP versus standard care, using the primary outcome measure of cost to diagnostic scan report calculated using hospital episode statistics (HES), with secondary outcome measures to assess the overall utility which include length of stay, time to diagnosis, overall cost of admission using HES, in-hospital complications, Patient Reported Outcome Measures (PROMs), readmission and re-attendance rates (ED/GP), and service/radiology costs.
Read the detailed description
Acute biliary disease comprises a significant proportion of surgical presentations in Accident and Emergency departments (A\&E), as well as of emergency surgical admissions to secondary care. Historically, this patient group first undergoes an abdominal ultrasound to confirm the presence of gallstones and look at ancillary features that may suggest cholecystitis or the presence of bile duct stones. The vast majority of patients who have abnormal liver biochemistry then proceed to Magnetic resonance cholangiopancreatography (MRCP), because the ultrasound scan is unable to clarify matters sufficiently to satisfy clinical need. There is often considerable delay in carrying out two sequential imaging investigations for each patient.
A number of studies have raised questions regarding the utility of ultrasound in acute biliary disease. The prevalence of Common Bile Duct (CBD) stones in patients with cholelithiasis is significant at 5-15%. CBD diameter, often used in US reporting as a marker of the presence of choledocholithiasis, may not correspond to the presence of a CBD stone - in one study, only 37% of patients with CBD stones had CBD dilatation on ultrasound. Ultrasound is a user-dependent technology, where the seniority of the scanner can influence the reliability of the report, and a 2013 study by Barlow et al. suggested that ultrasound findings in the context of deranged LFTs are often inaccurate in predicting CBD stones in gallstone pancreatitis, suggesting that MRCP be used to improve diagnosis. A 2015 retrospective study led by Qiu et al. found the sensitivity of peri-operative ultrasound for CBD stones to be very low at 44.95% and supported the use of MRCP as a diagnostic test if CBD stones were suspected. They also suggested the potential for economic benefits of using MRCP over US in patients with potential choledocholithiasis.
MRCP has been shown to be more cost-effective than US in selecting patients for Endoscopic Retrograde Cholangio-Pancreatography (ERCP) with suspected CBD stones, has a comparable accuracy to ERCP 6, and has been shown to reduce the number of unnecessary ERCPs performed in gallstone patients 7. Epelboym (2013) and Nebiker (2009) however disagree, characterising the use of MRCP in such patients as expensive and inefficient, and support the use of ultrasound as the primary diagnostic modality 8,9.
In a recent paper, Milburn et al conducted a retrospective study examining the patient journeys corresponding to 234 inpatient MRCP scans over a 2-year period. They found that increasing access to MRCP led to further interventions in 22% of cases due to an increased detection of complications and alternate pathologies (e.g. malignancy), and therefore increased overall length of stay. The median duration from request to scan was 2 days, with a further 1 day to scan report (therefore 3 days overall from request to report). They suggested improved access and timely reporting of MRCP could potentially reduce length of stay, though it may also increase the number of interventions 10. Clearly, there is a need to examine whether proceeding directly with MRCP (without preceding ultrasound) would prove to be cost-effective for these patients, and with a growing body of evidence as to the utility of early diagnosis to hasten the patient journey and improve treatment outcomes, further research is needed to determine whether the use of direct MRCP may be beneficial in this regard.
A recent audit of patients seen in the John Radcliffe Hospital ED over a period of six weeks revealed 46 patients admitted with gallstone disease, an incidence of approximately 1 admission per day. This correlates well with local audit of surgical admissions, which gives a referral rate of approximately 2 patients a day with 45% of patients referred from ED and 55% being referred from primary care. Despite the broad range of pathologies encountered in the ED and the considerable overlap in presentation, the diagnostic accuracy of emergency physicians with respect to gallstone disease was high, with the suggested specificity of an ED cholecystitis diagnosis calculated at around 85%, based largely on clinical findings and blood tests without radiological confirmation. This suggests that ED clinicians may be able to identify patients whose presenting symptoms are likely to be secondary to acute gallstone disease with a reasonable degree of accuracy on a clinical basis alone. Subsequent analysis of the continued inpatient diagnostic pathways suggested that whilst ultrasound remains the initial diagnostic radiological modality in the majority of patients with such presentations, approximately 59% (27/46) of patients undergo cross-sectional imaging during their admission, with around 48% (22/46) undergoing inpatient MRCP. Whilst access times to MRCP have improved in recent years, this pathway nevertheless may potentially result in an unnecessarily extended time to definitive diagnosis, and potentially unnecessary radiological expenditure. This raises the possibility that using MRCP as the initial diagnostic test in such patients may improve pathway efficiency, reduce length of stay and radiological burden, and hence reduce admission costs, notwithstanding the potential for improved diagnostic accuracy and detection of pathology such as common bile duct stones and/or pancreatitis. It may also improve patient satisfaction and clinical outcomes (e.g. earlier access to ERCP and stone removal in biliary obstruction patients). This can be assessed in a prospective randomised study to assess utility.
This pilot study aims to determine the utility of direct Magnetic Resonance Cholangiopancreatography (MRCP) in the assessment of suspected acute gallstone disease presentations. This will take the form of a randomized controlled trial, the design of which is based on recent internal audit data which indicated that a high proportion of patients ultimately require MRCP prior to diagnosis, treatment and discharge, and suggested that early scan may improve overall costs and outcomes. Patients with symptoms and signs suggestive of suspected gallstone disease and deranged liver function tests/amylase (i.e. suggestive of a potentially obstructive gallstone disease), will be enrolled across the full range of 'front-door' locations for surgical presentations within the hospital (Emergency Department, Surgical Emergency Unit, Ambulatory Assessment Unit), and randomized to one of two diagnostic pathways which are both existing variations in current clinical care:
- MRCP is used as the first mode of imaging;
- following a standard care model (ultrasound then MRCP if deemed appropriate). An assessment will then be undertaken of the cost-effectiveness of early MRCP versus standard care, using the primary outcome measure of cost to diagnostic scan report calculated using hospital episode statistics (HES), with secondary outcome measures to assess the overall utility which include length of stay, time to diagnosis, overall cost of admission using HES, in-hospital complications, Patient Reported Outcome Measures (PROMs), readmission and re-attendance rates, and service/radiology costs.
In addition to standard MRCP scan processing by the radiology department, data obtained through this study will be processed using the new quantitative MRCP+ technology (provided by Perspectum Diagnostics) to assess its diagnostic efficacy in detecting biliary tree dilatation, stones or strictures. Perspectum Diagnostics' quantitative MRCP technology is a software package which allows previously acquired MRCP data to be enhanced and quantitatively characterised using advanced image processing techniques (MRCP+). Conventional MRCP scans can be difficult to interpret since the 2D representation suffers from occlusion problems and a lack of depth information. This new technology can enhance the data without the need for contrast agent, enabling the visualization of smaller ducts. Quantitative characterisation of the biliary tree computes biliary tube diameter at each point along the duct, along with information about the cross-section orientation and branching topology. Combining true 3D rendering of the enhanced data with quantitative characterization facilitates clear mapping of the biliary tree, which can potentially improve surgical planning, facilitate detection of strictures, dilatations and gallstones in suspected biliary colic presentations and objectively stratify patients. As yet however this application of the MRCP+ has not been fully assessed in clinical practice, and this subsequent part of the study would aim to address this and provide data to enable assessment of its diagnostic utility.
- Being tested
- magnetic resonance cholangiopancreatography (MRCP)
- Medical subject headings
- Cholecystitis, Choledocholithiasis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
magnetic resonance cholangiopancreatography (MRCP)Diagnostic test
magnetic resonance imaging of liver, gall bladder, pancreas
| Study group | Role | What they receive |
|---|---|---|
| Standard Care | No intervention | Patients with suspected acute gallstone disease and deranged liver function tests/amylase will be investigated with abdominal ultrasound as first line imaging, as per standard care |
| Direct MRCP | Experimental | Patients with suspected acute gallstone disease and deranged liver function tests/amylase will be investigated with magnetic resonance cholangiopancreatography (MRCP) as first-line imaging Receives: Diagnostic Test: magnetic resonance cholangiopancreatography (MRCP) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Cost to diagnosis
Total cost of admission up to the final diagnostic scan report
Measured: 3 months
Secondary outcomes (5)
Overall cost of admission
Mean total cost of hospital admission for patients undergoing direct MRCP
Measured: 3 months
Length of stay
Mean length of hospital admission for patients undergoing direct MRCP
Measured: 3 months
Time to final diagnostic scan report
Mean time to final diagnostic scan report for patients undergoing direct MRCP
Measured: 3 months
In-hospital complications
Percentage rate of patient-reported significant 30-day complications throughout study duration
Measured: 3 months
readmission and re-attendance rates
Percentage rate of readmission/re-attendance throughout study duration
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Oct 2018
- Study start17 Jul 2019
- Primary completion31 Dec 2020
- Study completion31 Dec 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cholecystitis; Acute, CholedocholithiasisStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Randomised Controlled Trial
- Masking
- None (open label)
- Enrolment
- 27 participants (actual)
Sponsor and investigators
- Lead sponsor
- Perspectum
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Oxford University Hospitals NHS Trust
- Responsible party
- Sponsor
- Investigators
- Alex Novak, BSc MBChB, Principal investigator, Oxford University Hospitals NHS Trust
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03709030
- Sponsor's protocol ID
- 13946
- Acronym
- E-MAGED
- Status last verified
- May 2021
- First submitted
- 12 Oct 2018
- Last updated
- 6 May 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Novak A, Acharya A, Beer S, Espinosa A, Smith GB, Saga C, Andrews J, Bailey A, Soonawalla Z, Bungay H, Pavlides M. Pilot feasibility study to determine the utility of direct access and quantitative magnetic resonance cholangiopancreatography (MRCP) in the assessment of suspected acute biliary or ductal gallstone presentations. BMC Gastroenterol. 2025 Feb 10;25(1):72. doi: 10.1186/s12876-025-03637-0.
PubMed 39930378
Study at a glance
From the registry record, last updated by the sponsor on 6 May 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Determining the Utility of Direct Access Magnetic Resonance Cholangiopancreatography (MRCP) in the Assessment of Suspected Acute Gallstone Disease Presentations
- ClinicalTrials.gov ID
- NCT03709030
- Acronym / sponsor ID
- E-MAGED / 13946
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 27 participants (actual)
- Lead sponsor
- PerspectumIndustry (pharma, biotech, devices)
- Collaborators
- Oxford University Hospitals NHS Trust
- Study start
- 17 Jul 2019 (actual)
- Primary completion
- 31 Dec 2020 (actual)
- Study completion
- 31 Dec 2020 (actual)
- First posted
- 17 Oct 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.
This pilot study aims to determine the utility of direct Magnetic Resonance Cholangiopancreatography (MRCP) in the assessment of suspected acute gallstone disease presentations. This will take the form of a randomized controlled trial, the design of which is based on recent internal audit data which indicated that a high proportion of patients ultimately require MRCP prior to diagnosis, treatment and discharge, and suggested that early scan may improve overall costs and outcomes. Patients with symptoms and signs suggestive of suspected gallstone disease and deranged liver function tests/amylase (i.e. suggestive of a potentially obstructive gallstone disease), will be enrolled across the full range of 'front-door' locations for surgical presentations within the hospital (Emergency Department, Surgical Emergency Unit, Ambulatory Assessment Unit), and randomized to one of two diagnostic pathways which are both existing variations in current clinical care:
- MRCP is used as the first mode of imaging;
- following a standard care model (ultrasound then MRCP if deemed appropriate). An assessment will then be undertaken of the cost-effectiveness of early MRCP versus standard care, using the primary outcome measure of cost to diagnostic scan report calculated using hospital episode statistics (HES), with secondary outcome measures to assess the overall utility which include length of stay, time to diagnosis, overall cost of admission using HES, in-hospital complications, Patient Reported Outcome Measures (PROMs), readmission and re-attendance rates (ED/GP), and service/radiology costs.
Detailed description
Acute biliary disease comprises a significant proportion of surgical presentations in Accident and Emergency departments (A\&E), as well as of emergency surgical admissions to secondary care. Historically, this patient group first undergoes an abdominal ultrasound to confirm the presence of gallstones and look at ancillary features that may suggest cholecystitis or the presence of bile duct stones. The vast majority of patients who have abnormal liver biochemistry then proceed to Magnetic resonance cholangiopancreatography (MRCP), because the ultrasound scan is unable to clarify matters sufficiently to satisfy clinical need. There is often considerable delay in carrying out two sequential imaging investigations for each patient.
A number of studies have raised questions regarding the utility of ultrasound in acute biliary disease. The prevalence of Common Bile Duct (CBD) stones in patients with cholelithiasis is significant at 5-15%. CBD diameter, often used in US reporting as a marker of the presence of choledocholithiasis, may not correspond to the presence of a CBD stone - in one study, only 37% of patients with CBD stones had CBD dilatation on ultrasound. Ultrasound is a user-dependent technology, where the seniority of the scanner can influence the reliability of the report, and a 2013 study by Barlow et al. suggested that ultrasound findings in the context of deranged LFTs are often inaccurate in predicting CBD stones in gallstone pancreatitis, suggesting that MRCP be used to improve diagnosis. A 2015 retrospective study led by Qiu et al. found the sensitivity of peri-operative ultrasound for CBD stones to be very low at 44.95% and supported the use of MRCP as a diagnostic test if CBD stones were suspected. They also suggested the potential for economic benefits of using MRCP over US in patients with potential choledocholithiasis.
MRCP has been shown to be more cost-effective than US in selecting patients for Endoscopic Retrograde Cholangio-Pancreatography (ERCP) with suspected CBD stones, has a comparable accuracy to ERCP 6, and has been shown to reduce the number of unnecessary ERCPs performed in gallstone patients 7. Epelboym (2013) and Nebiker (2009) however disagree, characterising the use of MRCP in such patients as expensive and inefficient, and support the use of ultrasound as the primary diagnostic modality 8,9.
In a recent paper, Milburn et al conducted a retrospective study examining the patient journeys corresponding to 234 inpatient MRCP scans over a 2-year period. They found that increasing access to MRCP led to further interventions in 22% of cases due to an increased detection of complications and alternate pathologies (e.g. malignancy), and therefore increased overall length of stay. The median duration from request to scan was 2 days, with a further 1 day to scan report (therefore 3 days overall from request to report). They suggested improved access and timely reporting of MRCP could potentially reduce length of stay, though it may also increase the number of interventions 10. Clearly, there is a need to examine whether proceeding directly with MRCP (without preceding ultrasound) would prove to be cost-effective for these patients, and with a growing body of evidence as to the utility of early diagnosis to hasten the patient journey and improve treatment outcomes, further research is needed to determine whether the use of direct MRCP may be beneficial in this regard.
A recent audit of patients seen in the John Radcliffe Hospital ED over a period of six weeks revealed 46 patients admitted with gallstone disease, an incidence of approximately 1 admission per day. This correlates well with local audit of surgical admissions, which gives a referral rate of approximately 2 patients a day with 45% of patients referred from ED and 55% being referred from primary care. Despite the broad range of pathologies encountered in the ED and the considerable overlap in presentation, the diagnostic accuracy of emergency physicians with respect to gallstone disease was high, with the suggested specificity of an ED cholecystitis diagnosis calculated at around 85%, based largely on clinical findings and blood tests without radiological confirmation. This suggests that ED clinicians may be able to identify patients whose presenting symptoms are likely to be secondary to acute gallstone disease with a reasonable degree of accuracy on a clinical basis alone. Subsequent analysis of the continued inpatient diagnostic pathways suggested that whilst ultrasound remains the initial diagnostic radiological modality in the majority of patients with such presentations, approximately 59% (27/46) of patients undergo cross-sectional imaging during their admission, with around 48% (22/46) undergoing inpatient MRCP. Whilst access times to MRCP have improved in recent years, this pathway nevertheless may potentially result in an unnecessarily extended time to definitive diagnosis, and potentially unnecessary radiological expenditure. This raises the possibility that using MRCP as the initial diagnostic test in such patients may improve pathway efficiency, reduce length of stay and radiological burden, and hence reduce admission costs, notwithstanding the potential for improved diagnostic accuracy and detection of pathology such as common bile duct stones and/or pancreatitis. It may also improve patient satisfaction and clinical outcomes (e.g. earlier access to ERCP and stone removal in biliary obstruction patients). This can be assessed in a prospective randomised study to assess utility.
This pilot study aims to determine the utility of direct Magnetic Resonance Cholangiopancreatography (MRCP) in the assessment of suspected acute gallstone disease presentations. This will take the form of a randomized controlled trial, the design of which is based on recent internal audit data which indicated that a high proportion of patients ultimately require MRCP prior to diagnosis, treatment and discharge, and suggested that early scan may improve overall costs and outcomes. Patients with symptoms and signs suggestive of suspected gallstone disease and deranged liver function tests/amylase (i.e. suggestive of a potentially obstructive gallstone disease), will be enrolled across the full range of 'front-door' locations for surgical presentations within the hospital (Emergency Department, Surgical Emergency Unit, Ambulatory Assessment Unit), and randomized to one of two diagnostic pathways which are both existing variations in current clinical care:
- MRCP is used as the first mode of imaging;
- following a standard care model (ultrasound then MRCP if deemed appropriate). An assessment will then be undertaken of the cost-effectiveness of early MRCP versus standard care, using the primary outcome measure of cost to diagnostic scan report calculated using hospital episode statistics (HES), with secondary outcome measures to assess the overall utility which include length of stay, time to diagnosis, overall cost of admission using HES, in-hospital complications, Patient Reported Outcome Measures (PROMs), readmission and re-attendance rates, and service/radiology costs.
In addition to standard MRCP scan processing by the radiology department, data obtained through this study will be processed using the new quantitative MRCP+ technology (provided by Perspectum Diagnostics) to assess its diagnostic efficacy in detecting biliary tree dilatation, stones or strictures. Perspectum Diagnostics' quantitative MRCP technology is a software package which allows previously acquired MRCP data to be enhanced and quantitatively characterised using advanced image processing techniques (MRCP+). Conventional MRCP scans can be difficult to interpret since the 2D representation suffers from occlusion problems and a lack of depth information. This new technology can enhance the data without the need for contrast agent, enabling the visualization of smaller ducts. Quantitative characterisation of the biliary tree computes biliary tube diameter at each point along the duct, along with information about the cross-section orientation and branching topology. Combining true 3D rendering of the enhanced data with quantitative characterization facilitates clear mapping of the biliary tree, which can potentially improve surgical planning, facilitate detection of strictures, dilatations and gallstones in suspected biliary colic presentations and objectively stratify patients. As yet however this application of the MRCP+ has not been fully assessed in clinical practice, and this subsequent part of the study would aim to address this and provide data to enable assessment of its diagnostic utility.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Randomised Controlled Trial
| Arm | Type | Receives |
|---|---|---|
| Standard Care | No intervention | –Patients with suspected acute gallstone disease and deranged liver function tests/amylase will be investigated with abdominal ultrasound as first line imaging, as per standard care |
| Direct MRCP | Experimental | Diagnostic Test: magnetic resonance cholangiopancreatography (MRCP)Patients with suspected acute gallstone disease and deranged liver function tests/amylase will be investigated with magnetic resonance cholangiopancreatography (MRCP) as first-line imaging |
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (9 listed)
- Participant is willing and able to give informed consent for participation in the study.
- Male or Female, aged 16 years or above.
- Suspected gallstone/biliary disease presenting with acute abdominal pain AND
- At least one of the following blood test results to reflect abnormal liver function;
Key exclusion criteria (7 listed)
- Pregnant or nursing (lactating) women
- Previous diagnosis of chronic pancreatitis/hepatitis or chronic alcohol abuse
- Patients with contraindications to MR imaging
- Unstable disease as per judgment of the investigator which would render the patient unsuitable for MR imaging
- If not suitable for study intervention on admission - e.g. requiring immediate ERCP/surgery, or ICU admission
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 |
|---|---|---|
| magnetic resonance cholangiopancreatography (MRCP)magnetic resonance imaging of liver, gall bladder, pancreas | Diagnostic test | Direct MRCP |
Primary outcome
Cost to diagnosis
Time frame: 3 months
Total cost of admission up to the final diagnostic scan report
5 secondary outcomes
Overall cost of admission
Time frame: 3 months
Length of stay
Time frame: 3 months
Time to final diagnostic scan report
Time frame: 3 months
In-hospital complications
Time frame: 3 months
readmission and re-attendance rates
Time frame: 3 months
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 6 May 2021.
- Derived from this study: PubMed 39930378Novak A, Acharya A, Beer S, Espinosa A, Smith GB, Saga C, Andrews J, Bailey A, Soonawalla Z, Bungay H, Pavlides M. Pilot feasibility study to determine the utility of direct access and quantitative magnetic resonance cholangiopancreatography (MRCP) in the assessment of suspected acute biliary or ductal gallstone presentations. BMC Gastroenterol. 2025 Feb 10;25(1):72. doi: 10.1186/s12876-025-03637-0.
- Individual participant dataSharing planned: No
Related trials for Cholecystitis; Acute, Choledocholithiasis
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Cholecystectomy, Gallbladder
Not yet recruiting
Modified Laparoscopic Transcystic Biliary Drainage in the Management of Cholecystocholedocholithiasis
Common Bile Duct Calculi, Acute; Cholecystitis, Choledocholithiasis
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.
Alex Novak, BSc MBChB principal investigator
Oxford University Hospitals NHS Trust
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing magnetic resonance cholangiopancreatography (MRCP) in people with Cholecystitis; Acute, Choledocholithiasis, run by Perspectum at 1 site 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 9 inclusion and 7 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 6 May 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site 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?
Cost to diagnosis (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03709030, which also lists 1 linked publication.
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 6 May 2021.