RecruitingPhase 3NCT06017284

Thalidomide to Chemotherapy Related Nausea and Vomiting in Pancreatic Cancer


Sponsor

Fudan University

Enrollment

100 participants

Start Date

Nov 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the efficacy of thalidomide on improving the quality of life for metastatic pancreatic cancer patients receiving gemcitabine and nab-paclitaxel chemotherapy.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This trial tests whether thalidomide (a medication with anti-nausea properties) can reduce severe nausea and vomiting caused by chemotherapy in patients with metastatic pancreatic cancer. **You may be eligible if...** - You are between 18 and 80 years old - You have confirmed metastatic pancreatic cancer (adenocarcinoma) - You have not yet received any anti-cancer treatment - Your organs are functioning well enough (based on blood tests) - You are functioning reasonably well in daily life (ECOG 0–2) - You agree to use contraception during the study **You may NOT be eligible if...** - You have already received any cancer treatment - Your pancreatic cancer is not adenocarcinoma - You are pregnant or breastfeeding - You have active gut inflammation (pancreatitis, cholecystitis, etc.) - You have uncontrolled diabetes, high blood pressure, serious heart disease, or recent stroke - You are allergic to gemcitabine or nab-paclitaxel Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGThalidomide

Thalidomide 100 mg/day, once a day, orally intake at night.

DRUGNab paclitaxel

nab-paclitaxel (120 mg per square meter of body-surface area) on days 1, 8, and 15 every 4 weeks.

DRUGGemcitabine

gemcitabine (1000 mg per square meter) on days 1, 8, and 15 every 4 weeks.

DRUGPlacebo

Placebo, 100 mg/day, once a day, orally intake at night.


Locations(1)

Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

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NCT06017284


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