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Trials / Completed

CompletedNCT02430610

Irreversible Electroporation(IRE) For Uterine Cervical Neoplasms

Irreversible Electroporation(IRE) For Unresectable Uterine Cervical Neoplasms: Phase I and Phase II Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Fuda Cancer Hospital, Guangzhou · Academic / Other
Sex
All
Age
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate the safety and efficacy of irreversible electroporation (IRE) for unresectable Uterine Cervical Neoplasms.

Detailed description

By enrolling patients with unresectable Uterine Cervical Neoplasms adapted to enrolled criteria, this study will document for the first time the safety and the short and long term efficacy of percutaneous IRE for unresectable Uterine Cervical Neoplasms.

Conditions

Interventions

TypeNameDescription
PROCEDUREIrreversible electroporation (IRE)Irreversible Electroportion For Unresectable Uterine Cervical Neoplasms guide with ultrasound or/and CT.
DEVICENanoKnife

Timeline

Start date
2015-01-01
Primary completion
2020-12-01
Completion
2021-02-01
First posted
2015-04-30
Last updated
2021-09-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02430610. Inclusion in this directory is not an endorsement.

Irreversible Electroporation(IRE) For Uterine Cervical Neoplasms (NCT02430610) · Clinical Trials Directory