<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2012</study_start_year><condition>Fatty Liver</condition><condition>Steatohepatitis</condition><condition>Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><condition>first-line palliative treated, KRAS-Wild-Type, metastatic colorectal cancer</condition><disease>Fatty Liver</disease><disease>Steatohepatitis</disease><disease>Colorectal Cancer</disease><disease>First-line Palliative Treated, Kras-wild-type, Metastatic Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2119641</full_dataset_link><location>Austria</location><study_start_month>4</study_start_month><keyword>5-fluorouracil</keyword><keyword>Irinotecan</keyword><keyword>Chemotherapy</keyword><keyword>Folinic acid (Leucovorin)</keyword><keyword>Placebo</keyword><keyword>KRAS-Wild-Type</keyword><keyword>Metformin</keyword><keyword>Cetuximab</keyword><keyword>Metastatic colorectal cancer</keyword><keyword>Steatosis</keyword><keyword>Liver injury</keyword><repository>ECRIN MDR</repository><study_status>Terminated</study_status></additional><is_claimable>false</is_claimable><name>A Randomized, Placebo-controlled, Double-blind Phase II Study Evaluating if Glucophage Can Avoid Liver Injury Due to Chemotherapy Associated Steatosis</name><description>This multicenter randomized, placebo-controlled phase II study will enroll 132 first-line palliative treated subjects with metastatic KRAS wild type CRC. Subjects with histologically confirmed, KRAS wild-type CRC without previous chemo-therapy for metastatic disease will be screened for this study.
Approximately 10 sites in Austria will participate in the study. Subjects will be randomized in a ratio of 1:1 into two groups.</description><dates><creation>2012-04-15</creation></dates><accession>2119641</accession><cross_references><ClinicalTrials___gov>NCT01523639</ClinicalTrials___gov><EU Clinical Trials Register>2011-001010-34</EU Clinical Trials Register></cross_references></HashMap>