Clinical Trials Directory

Trials / Terminated

TerminatedNCT00584207

Radiofrequency Ablation of Uterine Fibroids

Status
Terminated
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
15 (actual)
Sponsor
University of California, Davis · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This research study is being conducted to evaluate the safety and effectiveness of ablation (destruction) of uterine leiomyomas (fibroids) using electrocautery heating guided by ultrasound. We are doing this to look for a less invasive method of treatment for patients with uterine fibroids. One method that is being used in other areas of the body to treat masses is radiofrequency electrocautery. This method may be performed for the treatment of uterine fibroids by placing a small diameter needle through the wall of the vagina into the fibroid guided by an ultrasound probe. An optional approach is to place the needle through the skin of the abdomen into the fibroid guided by an ultrasound probe. Once the needle is in the fibroid, the electrocautery current is applied and the fibroid is destroyed by heating. This would be done before hysterectomy (removal of the uterus). We are trying to test to see if this type of treatment can be applied to uterine fibroids. We are trying to develop radiofrequency electrocautery as one of the methods to treat fibroids without surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREradiofrequency ablationIntraoperative RFA of uterine fibroids

Timeline

Start date
2004-03-01
Primary completion
2007-03-01
Completion
2008-07-01
First posted
2008-01-02
Last updated
2009-04-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00584207. Inclusion in this directory is not an endorsement.