Actively Recruiting

Phase 2
Phase 3
Age: 18Years - 80Years
All Genders
NCT06601283

Vitamin C Plus Cordyceps to Chemotherapy Related Anemia in Pancreatic Cancer

Led by Fudan University · Updated on 2024-11-26

50

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate the efficacy of low-dose vitamin C plus herbal medicine on improving the quality of life for metastatic pancreatic cancer patients receiving gemcitabine and nab-paclitaxel chemotherapy.

CONDITIONS

Official Title

Vitamin C Plus Cordyceps to Chemotherapy Related Anemia in Pancreatic Cancer

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to understand and willing to sign informed consent
  • Age 18 to 80 years
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-2
  • Histologically or cytologically confirmed metastatic pancreatic adenocarcinoma
  • Adequate organ function based on laboratory tests
  • At least one measurable lesion according to RECIST criteria
  • Hemoglobin level of 8 g/dL or higher
  • Expected survival of at least 3 months
  • Women of childbearing potential and men must agree to use adequate contraception during the study
Not Eligible

You will not qualify if you...

  • Received anti-tumor treatment for other cancers in the last 2 years
  • Previously received any anti-tumor therapy for pancreatic cancer
  • Diagnosis of non-adenocarcinoma pancreatic cancer
  • Inflammation of the digestive tract such as pancreatitis, cholecystitis, or cholangitis
  • Pregnant or nursing women
  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency
  • Severe uncontrolled diseases including infections, diabetes, hypertension, or heart conditions (Class III or IV heart failure, recent myocardial infarction, unstable arrhythmia or angina, recent cerebral infarction)
  • Kidney failure or dialysis
  • Allergic reactions to gemcitabine, nab-paclitaxel, or related agents
  • Other serious illnesses that may affect safety or study compliance
  • Unwilling or unable to follow study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai Cancer Center

Shanghai, China, 200032

Actively Recruiting

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Research Team

H

Huanyu Xia, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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