Quantification of Pain Relief With Gonadal Vein Embolization for Pelvic Congestion Syndrome

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The primary objective is to quantify the degree of pain relief in patients undergoing gonadal vein embolization with coils as well as identify clinical or imaging factors that are predictive of a positive response to treatment, or poor response to treatment.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: No
View:

• Female patients 18 years of age or older

• Meet the clinical and imaging criteria for the diagnosis of PCS and have no contraindications to coil embolization of the gonadal veins.

• Patients who are treated with coil embolization of the gonadal veins in the Interventional Radiology division between October 1, 2018 to October 1, 2019.

Locations
United States
Kansas
The University of Kansas Medical Center
Recruiting
Kansas City
Contact Information
Primary
Carissa Walter, MPH
cwalter2@kumc.edu
9139457450
Time Frame
Start Date: May 10, 2019
Estimated Completion Date: September 25, 2024
Participants
Target number of participants: 30
Authors
Adam S Alli, Philip Johnson, Steven Lemons, Brandon Custer, Daniel Kirkpatrick, Zachary Collins
Related Therapeutic Areas
Sponsors
Leads: University of Kansas Medical Center

This content was sourced from clinicaltrials.gov

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