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Effectiveness of Low Dose Aspirin in Decreasing the Chance Getting Stomach and Intestine Cancer

Effectiveness of Low-dose Aspirin in Gastrointestinal Cancer Prevention - Hong Kong

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04081831
Acronym
ENgAGE-HK
Enrollment
99999
Registered
2019-09-09
Start date
2019-07-31
Completion date
2020-08-25
Last updated
2022-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal Cancer

Keywords

Esophageal cancer, Gastric cancer, Colorectal cancer

Brief summary

In this study, researchers wanted to learn more about the effect of Aspirin taken as low dose (75 - 300 mg) in preventing stomach, colorectal and esophagus cancer. The researchers were interested in the effect by duration of aspirin use and the effect on the time since aspirin intake has been stopped in preventing stomach, colorectal and esophagus cancer. In addition, the study also looked into the time patients survived after being diagnosed (survival rate) with cancer and number of cancer patients who died (case fatality rate). The study was based on an electronic database managed by the Health Authority in Hong Kong containing anonymized clinical information of patients living in Hong Kong.

Interventions

Follow clinical administration

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- Received prescription of either low-dose aspirin (75-300 mg) or paracetamol monotherapy during enrolment period.

Exclusion criteria

* Received prescription of aspirin monotherapy or combination one year prior to the index date * Recorded diagnoses of any type of cancer before the index date * Recorded procedures of colectomy, gastrectomy prior to the index date * Age \< 40 years

Design outcomes

Primary

MeasureTime frameDescription
Incidence rate ratio of colorectal cancer among users of low-dose-aspirin (exposed) and users of paracetamol monotherapy (non-exposed)Retrospective analysis between 1st January 2004 and 31st December 2008Ratio of incidence (per 10,000 person years) among users of low-dose-aspirin (exposed) and users of paracetamol monotherapy (non-exposed)
Incidence rate ratio of gastric cancer among users of low-dose-aspirin (exposed) and users of paracetamol monotherapy (non-exposed)Retrospective analysis between 1st January 2004 and 31st December 2008Ratio of incidence (per 10,000 person years) among users of low-dose-aspirin (exposed) and users of paracetamol monotherapy (non-exposed)
Incidence rate ratio of esophageal cancer among users of low-dose-aspirin (exposed) and users of paracetamol monotherapy (non-exposed)Retrospective analysis between 1st January 2004 and 31st December 2008Ratio of incidence (per 10,000 person years) among users of low-dose-aspirin (exposed) and users of paracetamol monotherapy (non-exposed)

Secondary

MeasureTime frameDescription
Case-fatality and survival rateRetrospective analysis between 1st January 2004 and 31st December 2008For colorectal cancer, gastric or oesophageal
Duration of aspirin useRetrospective analysis between 1st January 2004 and 31st December 2008Minimum duration of aspirin use to confer the protective effects in preventing colorectal, gastric and esophageal cancer
Risk of colorectal, gastric and esophageal cancer after discontinuation of aspirin useRetrospective analysis between 1st January 2004 and 31st December 2008Logistic regression will be conducted based on nested case-control study with stratification on the recency of exposure with current use, past use, and distant use of aspirin.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026