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NCT03326791CompletedPhase 2/3

Aspirin in Colorectal Cancer Liver Metastases

Acetylsalicylic Acid as Secondary Prevention in Colorectal Cancer

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

The ASAC trial is a Scandinavian, multi-center, double-blinded, randomized, placebo-controlled study to determine whether adjuvant treatment with low-dose acetylsalicylic acid (ASA) can improve disease free survival in patients treated with resection for colorectal cancer liver metastases (CRCLM). Several studies have shown beneficial effect of ASA on primary prevention of CRC and the investigators group and others have shown a potential association of ASA also taken after the diagnosis on CRC survival in registry-based studies (secondary prevention). Up to 800 patients operated for CRCLM will be randomized to Arm#1 ASA 160 mg once daily or Arm#2 Placebo for a period of 3 years or till disease recurrence. The patients will be treated and followed up according to standard of care and the National Guidelines. The ASAC trial will be the first clinical interventional trial to assess the beneficial role of ASA in recurrence of CRC liver metastases and survival. ASA is an inexpensive, well tolerated, and easily accessible drug that will be highly potential as adjuvant drug in secondary prevention of CRC liver metastases if the study shows a beneficial effect. This trial will also investigate the effect of ASA as adjuvant treatment on Health-related Quality of Life and the cost-effectiveness.

Status (registry)
Completed
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
466 (actual)
First submitted
2 Oct 2017
Start date
15 Dec 2017
Primary completion date
1 Feb 2022
Lead sponsor
Oslo University Hospital
NCT number
NCT03326791

What you commit to

  • Study type: Interventional · Phase 2/3
  • Participants enrolled: 466
  • From 15 Dec 2017 to the primary completion date, 1 Feb 2022
  • 14 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Ongoing regular use of corticosteroids or NSAIDs.
  • CRCLM previously treated with radiofrequency or microwave ablation technique
  • Contraindication listed on the Summary of Product Characteristics (SmPC) of Trombyl: Hypersensitivity/allergies to ASA, Thrombocytopenia, Previous severe gastrointestinal haemorrhage/peptic ulcer due to ASA/NSAID, Active peptic ulcer, Haemophilia, Liver cirrhosis, Severe congestive heart failure.
  • Need to use concomitant medications contraindicated according to SmPC of Trombyl.

Other illness

  • Severe heart failure (classified as New York Heart Association (NYHA) class \>III)
  • Severe kidney failure \>Stage 3b

Lab values

  • Concomitant use of ASA or other anticoagulants or platelet inhibitors such as warfarin or clopidogrel.
  • Blood platelets (thrombocytes) \< 100 x 10\^9/L.

Age

  • Pregnancy or breastfeeding. For women in childbearing age there will be pregnancy test at monthly intervals (urine human chorionic gonadotropin (HCG) pregnancy tests (for home testing) will be given to the patients for monthly tests and the patient will self-report the results at each control). Furthermore, highly effective contraceptives will be required.

Other

  • Inherited or acquired coagulopathy (haemophilia).
  • Childbearing potential without proper contraceptive measures such as oral contraceptives, other hormonal contraceptives (vaginal products, skin patches, or implanted or injectable products), or mechanical products such as an intrauterine device to avoid pregnancy for the entire study period.
  • Liver cirrhosis with a Child-Pugh score \>B7.
  • Alcoholism.

Who the study is looking for

  • First time CRCLM (synchronous or metachronous).
  • Recurrence of CRCLM (not previously included in this trial).
  • In synchronous CRCLM and "Liver first" approach, the primary tumor must be resected within 6 weeks after the liver
  • Macroscopic (surgical) free resection margins (R0 or R1 resection).
  • Must be ambulatory with a performance status Eastern Cooperative Oncology Group (ECOG) 0-2.
  • Must be at least 18 years of age.
  • Signed informed consent and expected cooperation of the patients for the treatment and follow up must be obtained and documented according to International Conference on Harmonization - Good Clinical Practice (ICH GCP), and national/local regulations.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (14)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Aarhus University Hospital
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AarhusDenmarkUnknown status
Rigshospitalet, Copenhagen
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CopenhagenDenmarkUnknown status
Odense University Hospital
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OdenseDenmarkUnknown status
Haukeland University Hospital
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BergenNorwayUnknown status
Oslo University Hospital
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OsloNorwayUnknown status
Stavanger University Hospital
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StavangerNorwayUnknown status
University Hospital of North Norway
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TromsøNorwayUnknown status
St Olavs Hospital
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TrondheimNorwayUnknown status
Sahlgranska University Hospital
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GothenburgSwedenUnknown status
Linkoping University Hospital
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LinköpingSwedenUnknown status
Skåne University Hospital Lund
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LundSwedenUnknown status
Karolinska University Hospital
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StockholmSwedenUnknown status
University Hospital of Umeå
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UmeåSwedenUnknown status
Uppsala University Hospital
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UppsalaSwedenUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.