Clinical Trials Directory

Trials / Completed

CompletedNCT02981719

Simultaneous Gemcitabine and Irreversible Electroporation for Locally Advanced Pancreatic Cancer

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
61 (actual)
Sponsor
Fuda Cancer Hospital, Guangzhou · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The aim of this study was to compare the therapeutic efficacy between simultaneous gemcitabine administration and IRE and IRE alone for locally advanced pancreatic cancer (LAPC)

Detailed description

in the GEM- IRE group, before the IRE ablation started, patients received 1000 mg/m2 gemcitabine hydrochloride \[Qilu pharmaceutical (Hainan) Co., Ltd. Haikou, China\] intravenously (over approximately 30 min). In the IRE group, the IRE ablation was performed without gemcitabine intravenous infusion before IRE. The aim of this study was to evslusted the overall survival (OS), objective response rate (ORR) and adverse events after simultaneous therapy.

Conditions

Interventions

TypeNameDescription
PROCEDUREsimultaneous gemcitabine and irreversible electroporationgemcitabine intravenous infusion prior to irreversible electroporation treatment
PROCEDUREirreversible electroporationpercutaneous irreversible electroporation was performmed for locally advaanced pancreatic cancer.

Timeline

Start date
2016-10-01
Primary completion
2018-10-01
Completion
2020-10-01
First posted
2016-12-05
Last updated
2021-01-22

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02981719. Inclusion in this directory is not an endorsement.