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Evaluation study on screening of upper gastrointestinal cancer in China: a randomized controlled trial

evaluation on screening of upper gastrointestinal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-EOR-16008577
Enrollment
Unknown
Registered
2016-06-01
Start date
2015-06-01
Completion date
Unknown
Last updated
2022-10-24

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

Conditions

upper gastrointestinal cancer

Interventions

1:endoscopic examination

Sponsors

NATIONAL CANCER CENTER OF CHINA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 69 Years

Inclusion criteria

Inclusion criteria: A total of seven cities/counties would be selected as the screening centers, covering areas with high incidence of upper gastrointestinal cancer and middle/low incidence rates. Multi-center cluster based randomization would be used. Cases and controls will be 1:1 matched. In areas with high incidence of upper gastrointestinal cancer, 60 000 subjects will be enrolled. In areas with middle/low incidence of upper gastrointestinal cancer, 80 000 subjects will be enrolled. The areas with high risk of uppergastrointestinal cancer are located at: Linzhou County of Henan Province, Cixian County of Hebei Province, Wuwei County of Gansu Province. The areas with middle/low risk of uppergastrointestinal cancer are located at: Sheyang County of Jiangsu Province, Luoshan County of Henan Province, Harbin City of Heilongjiang Province. The inclusion criteria includes: local residents aged 40-69, no history of cancer, no history of endoscopic examination in the latest 3 years, willing to accept endoscopic examination.

Exclusion criteria

Exclusion criteria: 1. Subjects with history of cancer or severe diseases who are tolerate endoscopic examination; 2. Subjects who are not willing to take endoscopic examination; 3. Men and women who at the time of randomization are 69 years of age; 4. Individuals currently undergoing treatment for cancer; 5. Individuals who had uppergastrointestinal endoscope in the past three years; 6. Individuals who are unwilling to sign the consent form.

Design outcomes

Primary

MeasureTime frame
mortality rate;

Secondary

MeasureTime frame
detection rate;incidence rate;survival rate;stage;Cost benefit ratio;Cost-Effectiveness Ratio;QUALITY ADJUSTED LIFE YEAR;DISABILITY ADJUSTED LIFE YEAR;

Countries

China

Contacts

Public ContactWANQING CHEN

NATIONAL CANCER CENTER OF CHINA

chenwq@cicams.ac.cn+86 10 87787039

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 27, 2026