Clinical Trials Directory

Trials / Terminated

TerminatedNCT04073485

Microwave Ablation for Uterine Fibroids

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
6 (actual)
Sponsor
Chinese University of Hong Kong · Academic / Other
Sex
Female
Age
30 Years – 50 Years
Healthy volunteers
Not accepted

Summary

This study is aimed to evaluate the clinical safety and effectiveness of Microwave ablation (MWA) in treating patients with uterine fibroid.

Detailed description

Percutaneous radiofrequency ablation (RFA) is another form of thermal ablation that has been used for the treatment of uterine fibroids. Although RFA is more invasive when compared to High-Intensity-Focused-Ultrasound (HIFU), the treatment is less limited by the location of the lesions, and the treatment procedure is more time efficient. To further improve the technology of thermal ablation for uterine fibroid, percutaneous microwave ablation (MWA) could be a promising option because it allows increased efficiency of energy transmission and reduction in procedure time, and may allow effective treatment of large lesions.

Conditions

Interventions

TypeNameDescription
PROCEDUREMicrowave ablationUltrasonogram is performed to identify the fibroid or adenomyoma. A trocar needle is placed into the lesion under local anesthesia. The MWA procedure is performed using appropriate microwave power and application time are selected to provide sufficient ablation coverage to the target lesion.

Timeline

Start date
2019-09-05
Primary completion
2023-03-09
Completion
2023-03-31
First posted
2019-08-29
Last updated
2023-05-03

Locations

1 site across 1 country: Hong Kong

Source: ClinicalTrials.gov record NCT04073485. Inclusion in this directory is not an endorsement.