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To explore the effect of early whole course immune nutrition supplementation in patients with previously untreated advanced pancreatic cancer:a prospective, single-arm, single-center clinical study

To explore the effect of early whole course immune nutrition supplementation in patients with previously untreated advanced pancreatic cancer:a prospective, single-arm, single-center clinical study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091619
Enrollment
Unknown
Registered
2024-10-31
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

pancreatic cancer

Interventions

Test group:1. Clinical anti-tumor treatment plan: According to the Chinese Guidelines for Diagnosis and Treatment of Pancreatic Cancer (2021 edition), oncologists will develop and implement standard a
500ml was taken orally daily (8.5g arginine, 0.9g nucleotide, and 2g omega-3 unsaturated fatty acids). The patient was given oral nutrition supplements (ONS) at 500ml/ day 1 to 3 days before the first

Sponsors

The Affiliated Drum Tower Hospital to Medical School of Nanjing University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Histologically or cytologically confirmed advanced pancreatic cancer (advanced pancreatic cancer is defined as local and/or distant metastases that cannot be surgically removed) 2. Not received systematic antitumor therapy before 3, Age 18-80 years old, gender unlimited 4. Eastern Cooperative Oncology (ECOG) has a baseline performance status of 0, 1, or 2 5. Life expectancy is more than 3 months 6. Clear mind, no communication barriers, can answer questions 7. Informed consent has been signed 8. Able to follow research protocols and follow-up procedures

Exclusion criteria

Exclusion criteria: 1. Allergies to certain nutrients 2. Participate in other clinical trials 3. Participants considered unsuitable for this experiment by the researchers 4. Subjects have concurrent or previous history of other tumors 5. Patients with peritoneal metastasis or ascites caused by tumor 6. Patients with infectious diseases, liver, kidney and other organ functions with serious abnormalities

Design outcomes

Primary

MeasureTime frame
Skeletal muscle index;

Secondary

MeasureTime frame
Patient quality of life score;Psychological score;Nutritional status;Cardiac function assessment;Peripheral blood biomarkers;1 year PFS rate;1 year OS rate;Safety;

Countries

China

Contacts

Public ContactDu Juan

The Affiliated Drum Tower Hospital to Medical School of Nanjing University

dujuanglyy@163.com+86 25 8310 6666

Outcome results

None listed

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