Blood test before surgery may predict stomach cancer survival
NCT ID NCT06686966
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether routine blood tests taken before surgery can help predict complications and long-term survival in people with gastric cancer. Researchers analyzed data from 3,400 patients across multiple hospitals. The goal was to create a simple tool that helps doctors identify high-risk patients and personalize treatment plans.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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3,400 people
The number who actually took part.
- Started
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Jan 2010
- Finished
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Nov 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients diagnosed with gastric cancer and undergoing radical gastric cancer surgery at the First Hospital of Chongqing Medical University, the Second Hospital of Chongqing Medical University, and the Yongchuan Hospital of Chongqing Medical University.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients aged ≥18 years; * patients diagnosed with gastric cancer by pathological biopsy before surgery; * patients without chemotherapy, radiotherapy, targeted and immunotherapy before enrolment; * willing to participate in this study and sign the informed consent; * complete clinical data. Exclusion Criteria: * patients with other primary malignant tumours other than gastric cancer; * patients with systemic diseases such as severe cardiopulmonary insufficiency that affect the choice of treatment plan; * patients who are not suitable for enrolment as assessed by the investigator; * incomplete clinical data.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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Other studies related to the condition(s) this trial covers.
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