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Dosage exploration of ratitrexed in HIPEC

Dosage exploration of ratitrexed in HIPEC

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044214
Enrollment
Unknown
Registered
2021-03-12
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Malignat tumor

Interventions

Different doses groups:Ratitrexed for HIPEC

Sponsors

Changzhou Second Peopel's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. Expected survival longer than 3 months; 3. Locally advanced or metastatic colorectal cancer diagnosed by histopathology and (or) cytology; 4. At least 4 weeks elapsed between the end of the last treatment; 5. ECOG score 0 -1; 6. The patient has good liver and kidney function; 7. The subjects volunteered to participate in the experiment and signed the informed consent; 8. Use reasonable methods of contraception during medication.

Exclusion criteria

Exclusion criteria: 1. Any of the following conditions occurred during the first 6 months of enrollment:myocardial infarction, angina pectoris, congestive heart failure, transient cerebral ischemia, etc.; 2. During the first 3 months of enrollment, any of the following conditions occurred: gastric or duodenal ulcer that did not respond to treatment, erosive esophagitis or gastritis, gastrointestinal perforation, inflammatory bowel disease, pulmonary embolism, or other uncontrolled thromboembolic events; 3. AIDS-related diseases; 4. The study did not agree to use reasonable methods of contraception during treatment; 5. Bone marrow insufficiency: hemoglobin < 8.0g/dL, neutrophils < 1.5x10^9/L, platelets < 90x10^9/L; 6. Laboratory tests revealed hepatic and function insufficiency; 7. Others that researchers think should be ruled out.

Design outcomes

Primary

MeasureTime frame
Blood drug concentration ;Adverse reaction;security;PFS;OS;

Countries

China

Contacts

Public ContactXiaolin Pu

Changzhou Second People's Hospital of Jiangsu Province

pxlin20021078@163.com+86 18551698622

Outcome results

None listed

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