NCT Number: NCT00192842
Gemcitabine With Curcumin for Pancreatic Cancer
The study hypotheasis is that curcumin, a natural compound with a potent antiproliferative effect, can improve the efficacy of the standard chemotherapy gemcitabine in patients with advanced pancreatic cancer. That is why the patients are given a daily oral dose of 8 gr of curcumin along the chemotherapeutic protocol of weekly gemcitabine.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- locally advanced or metastatic adenocarcinoma of the pancreas
- no prior chemotherapy
- performance status 0-2
- adequate hematology and chemistry
Exclusion criteria
- serious concurrent medical condition
Treatment and study plan
Primary outcomes
-
time to tumor progression
Secondary outcomes
-
response rate
-
survival
-
clinical benefit
-
toxicity
Sponsors and collaborators
Lead sponsor
Rambam Health Care Campus
Other
Registry information
Official study title
Phase II Trial of Gemcitabine and Curcumin in Patients With Advanced Pancreatic Cancer
Important dates
- Study start
- 2004
- Primary completion
- 2007
- Study completion
- 2010
- First posted
- Sep 19, 2005
- Registry last updated
- Sep 22, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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