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Recruiting Phase 2, Phase 3 NCT06598033

NCT06598033 Vitamin C Plus Cordyceps to Quality of Life in Patients With Terminal Stage Pancreatic Cancer

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Clinical Trial Summary
NCT ID NCT06598033
Status Recruiting
Phase Phase 2, Phase 3
Sponsor Fudan University
Condition Pancreatic Cancer
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2024-11-22
Primary Completion 2026-10-01

Trial Parameters

Condition Pancreatic Cancer
Sponsor Fudan University
Study Type INTERVENTIONAL
Phase Phase 2, Phase 3
Enrollment 50
Sex ALL
Min Age 18 Years
Max Age 80 Years
Start Date 2024-11-22
Completion 2026-10-01
Interventions
VC plus herbal medicine

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Brief Summary

The purpose of this study is to evaluate the efficacy of vitamin C plus herbal medicine in improving the quality of life for metastatic pancreatic cancer patients who are resistant to chemotherapy.

Eligibility Criteria

Inclusion Criteria: * • Ability to understand and the willingness to sign a written informed consent document. * Age ≥ 18 years and ≤ 80 years. * Eastern Cooperative Oncology Group (ECOG) performance status 0-2. * Histologically or cytologically confirmed metastatic pancreas adenocarcinoma. * Tumor progression after two lines of treatments. * Adequate organ performance based on laboratory blood tests. * Presence of at least of one measurable lesion in agreement to RECIST criteria. * The expected survival ≥ 1 months. * Women of childbearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation. Exclusion Criteria: * • The diagnosis was confirmed by pathology as non-adenocarcinoma of pancreas. * Inflammation of the digestive tract, including pancreatitis, cholecystitis, cholangitis, etc. * Pregnant or nursing women. * Glucose-6-phosphate dehydrogenase (G6PD) deficiency. * Severe and uncontrollable accompanying diseases

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