Skip to content

Capecitabine Effect in Non-metastatic Gastric Cancer Patients

Evaluation of Capecitabine Effect as Maintenance Chemotherapy in Non-metastatic Gastric Cancer Patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241228064191N1
Enrollment
60
Registered
2025-04-27
Start date
2025-03-21
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

nonmetastatic gastric cancer. Malignant neoplasm of stomach

Interventions

Intervention 1: Intervention group: Oral capecitabine (Rooyan daroo company, Rooyan AQVIDA line) at a dose of 1000 mg/m2 daily for two weeks in each three-week cycle (the patient does not take the dru

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who are adults and over 18 years of age Patients with non-metastatic gastric tumors Patients who received the FLOT regimen as neoadjuvant chemotherapy Patients who have undergone surgery and received chemotherapy after surgery

Exclusion criteria

Exclusion criteria: Patients with metastatic disease Patients who did not receive FLOT chemotherapy before surgery Patients who did not receive FLOT chemotherapy after surgery Non-metastatic patients who have not had surgery

Design outcomes

Primary

MeasureTime frame
Tumor recurrence. Timepoint: At the beginning of the study (before the intervention), the end of the third month, the end of the sixth month, the end of the ninth month, and the end of the twelfth month after beginning chemotherapy. Method of measurement: CT scan of the chest, abdomen, and pelvis with and without contrast medium or ultrasound (if CT scan is not possible).;Drug side effects. Timepoint: At the beginning of the study (before the intervention), the end of the third month, the end of the sixth month, the end of the ninth month, and the end of the twelfth month after beginning chemotherapy. Method of measurement: Drug side effects questionnaire.

Secondary

MeasureTime frame
Metastasis locations. Timepoint: At the beginning of the study (before the intervention), the end of the third month, the end of the sixth month, the end of the ninth month, and the end of the twelfth month after beginning chemotherapy. Method of measurement: CT scan of the chest, abdomen, and pelvis with and without contrast medium or ultrasound (if CT scan is not possible).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoghra Mohammadi

Shiraz University of Medical Sciences

shokoh9090@gmail.com+98 71 3230 5410

Outcome results

None listed

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