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Non-interventional study of apatinib in the treatment of esophageal cancer

Non-interventional study of apatinib in the treatment of esophageal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023814
Enrollment
Unknown
Registered
2019-06-13
Start date
2019-07-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

Esophageal cancer

Interventions

treatment group:apatinib

Sponsors

Shanxi Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged =18 years, male or female; 2. Patients diagnosed with esophageal cancer by histology or cytology; 3. Patients who the researchers believe benefit from treatment; 4. Subjects voluntarily participate in this study and sign the informed consent form (ICF); 5. Patients with compliance are expected to follow up the curative effect and adverse reactions as required by the protocol.

Exclusion criteria

Exclusion criteria: 1. Confirmed allergy to apatinib mesylate tablets and/or its excipients; 2. Pregnant or lactating women; 3. Contraindications of apatinib (patients with active bleeding, ulcer, intestinal perforation, intestinal obstruction, uncontrolled hypertension within 30 days after major operation, grade iii-iv cardiac insufficiency, severe liver and kidney insufficiency should not be allowed); 4. Other conditions considered unsuitable for inclusion by the researcher.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
Progression-free survival;

Countries

China

Contacts

Public ContactShiping Guo

Shanxi Cancer Hospital

hrkangruijun@163.com+86 18360697909

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026