Acute PresentatiOn of CoLorectaL Cancer: an internatiOnal Snapshot
NCT ID: NCT05641129
Last Updated: 2024-02-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2000 participants
OBSERVATIONAL
2023-01-16
2023-11-11
Brief Summary
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Detailed Description
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Secondary aims:
* Identify risk factors for mortality (intraoperatively, at 30-days and at 90-days) and ostomy rates (at 30- and 90-days) in patients deemed for active management (i.e., not for palliative management) to develop a risk prediction model
* Validate risk criteria of large bowel obstruction in patients with previously known colorectal cancer undergoing neoadjuvant chemotherapy or awaiting elective surgery
Who?
* Patients aged 18 years and above presenting to the hospital acutely with colorectal cancer (CRC) for malignant large bowel obstruction (LBO), perforation, CRC-related haemorrhage or other reasons within the data collection periods. Both those managed with and without surgery will be included
* Patients with localised and metastatic disease will be included
* Patients with known colorectal cancer diagnoses will be included if they present acutely (e.g., with disease progression)
* Patients presenting acutely for the side effects of chemotherapy/radiotherapy of known cancers will be excluded
What? Data will be collected on patients' presenting status and symptoms, patient management strategies, and intraoperative and postoperative outcomes.
When? Prospectively over 2023 in consecutive 6-week data collection blocks between January and June with 90-day follow-up till September.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Main Cohort
Consecutive adult patients (≥18 years of age) presenting acutely (i.e. unplanned and non-elective presentation to hospital for urgent or emergency reasons) for symptoms of known or unknown colorectal cancer assessed by hospital surgical teams. Patients should be included regardless of operative or non-operative management, and curative or palliative intent.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients who are operated on for curative/palliative treatment of colorectal cancer
* Patients who are referred to general surgery for assessment (irrespective of if they proceed to surgery)
* New diagnoses of colorectal cancer
* Extent of cancer: All patients including extra-abdominal metastatic, intra-abdominal metastatic and non-metastatic disease
* Known cancer: Patients presenting for the first time with colorectal cancer AND/OR known colorectal cancer diagnosis with progression of disease. i.e. obstruction of known colorectal cancer
* Patient presentation: Symptomatic presentation of colorectal cancer i.e. large bowel obstruction, haemorrhage, perforation
Exclusion Criteria
* Patients with secondary cancers
* Previously included in the study
18 Years
ALL
No
Sponsors
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European Student Research Network
NETWORK
Responsible Party
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Locations
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Aberdeen Royal Infirmary
Aberdeen, Ireland, United Kingdom
Countries
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References
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EuroSurg Collaborative and STARSurg Collaborative*. Global Use and Outcomes of Endoscopic Stenting in Acute Malignant Left-Sided Colonic Obstruction: A Secondary Analysis of APOLLO, An International, Prospective Cohort Study. Dis Colon Rectum. 2025 Oct 10. doi: 10.1097/DCR.0000000000003960. Online ahead of print.
Other Identifiers
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APOLLO Study
Identifier Type: -
Identifier Source: org_study_id
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