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NCT06598033RecruitingPhase 2/3

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

Source: ClinicalTrials.gov · Last updated 26 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
50 (estimated)
First submitted
11 Sept 2024
Start date
22 Nov 2024
Primary completion date
1 Oct 2026
Lead sponsor
Fudan University
NCT number
NCT06598033

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 50
  • From 22 Nov 2024 to the primary completion date, 1 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • • 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 that may affect protocol compliance or interfere with the interpretation of results.
    • Renal insufficiency or dialysis
    • Other serious accompanying illnesses, which, in the researcher\'s opinion, could seriously adversely affect the safety of the treatment.
    • Patients who are unwilling or unable to comply with study procedures.

Who the study is looking for

  • • 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.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Shanghai Cancer Center
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.